Title of Invention

"METHOD FOR MANUFACTURING A PERITONEAL DIALYSIS SOLUTION"

Abstract

A method for manufacturing a peritoneal dialysis solution, the method comprising: providing a glucose polymer; performing a bioburden test on the glucose polymer in an acidic medium and at an elevated temperature to detect contaminating Alcyclobacillus acidocaldarius; testing the glucose polymer with a reagent derived from silkworm larvae plasma, wherein the reagent is reactive with any peptidoglycan in the glucose polymer to determine a peptidoglycan concentration; and using the glucose polymer to prepare the peritoneal dialysis solution if the peptidoglycan concentration is determined to be about 10 ng/mL or less.

Full Text

SPECIFICATION TITLE OF THE INVENTION "METHODS AND COMPOSITIONS FOR DETECTION OF MICROBIAL CONTAMINANTS IN PERITONEAL DIALYSIS SOLUTIONS" BACKGROUND OF THE INVENTION The present invention generally relates to the detection of gram positive microbial contaminants. More specifically, the present invention relates to methods and compositions that employ the detection of peptidoglycan in peritoneal dialysis solutions. Peptidoglycans are major cell wall components of gram positive organisms and thus serve as a good marker of these microbes. Due to disease or insult or other causes, the renal system can fail. In renal failure of any cause, there are several physiological derangements. The balance of water, minerals (e.g., Na, K, Cl, Ca, P, Mg, SO) and the excretion of a daily metabolic load of fixed ions is no longer possible in renal failure. During renal failure, toxic end products of nitrogen metabolism (e.g., urea, creatinine, uric acid, and the like) can accumulate in blood and tissues. Dialysis processes have been devised for the separation of elements in a solution by diffusion across a semi-permeable membrane (diffusive solute transport) across a concentration gradient Examples of dialysis processes include hemodialysis, peritoneal dialysis and hemofiltration. Hemodialysis treatment utilizes the patient's blood to remove waste, toxins, and excess water from the patient. The patient is connected to a hemodialysis machine and the patient's blood is pumped through the machine. Catheters or the like are inserted into the patient's veins and arteries to connect the blood flow to and from the hemodialysis machine. Waste, toxins, and excess water are removed from the patient's blood and the blood is infused back into the patient. Hemodialysis treatments can last several hours and are generally performed in a treatment center about three or four times per week. To overcome the disadvantages often associated with classical hemodialysis, other techniques were developed, such as peritoneal dialysis. Peritoneal dialysis utilizes the patient's own peritoneum as a semipermeable membrane. The peritoneum is the membranous lining of the body cavity that, due to the large number of blood vessels and capillaries, is capable of acting as a natural semipermeable membrane. In peritoneal dialysis, a sterile dialysis solution is introduced into the peritoneal cavity utilizing a catheter or the like. After a sufficient period of time, an exchange of solutes between the dialysate and the blood is achieved. Fluid removal is achieved by providing a suitable osmotic gradient from the blood to the dialysate to permit water outflow from the blood. This allows a proper acid-base, electrolyte and fluid balance to be returned to the blood. The dialysis solution is simply drained from the body cavity through the catheter. Examples of different types of peritoneal dialysis include continuous ambulatory peritoneal dialysis, automated peritoneal dialysis and continuous flow peritoneal dialysis. Standard peritoneal dialysis solutions contain dextrose to effect transport of water and metabolic waste products across the peritoneum. Although dextrose has the advantage of being relatively safe and inexpensive, it has a number of disadvantages. Because of the small size, dextrose is rapidly transported through the peritoneum, thus leading to the loss of osmotic gradient and loss of ultrafiltration within about 2 to 4 hours of infusion. It has been suggested that the ultrafiltration characteristics of peritoneal dialysis solutions could be improved by replacing dextrose with large molecular weight substances, such as glucose polymers. An example of a novel high molecular weight agent is icodextrin. Dialysis solutions containing icodextrin are commercially available and have been found to be useful in treating patients with end stage renal disease. Peritonitis is a major complication of peritoneal dialysis. Clinical suspicion of peritonitis is prompted by thb development of a cloudy-appearing dialysate in combination with variable clinical manifestations that may include abdominal pain, nausea, vomiting, diarrhea and fever. See, for example, Vas SI: Peritonitis. In: Nolph KD, ed. Pentoneal Dialysis. 3rd ed. Dordrecht, The Netherlands: Kluwer Academic Publishers, 1989:261-84. Most episodes of peritonitis are caused by intraperitoneal bacterial infections, and the diagnosis is usually readily established by positive dialysate cultures. However, there are several well documented causes of non-infectious or sterile peritonitis. Aseptic or sterile peritonitis, which also is described as aseptic, chemical, or culture-negative peritonitis, is typically caused by a chemical or a foreign body irritant. One of the major outbreaks of sterile peritonitis among patients on peritoneal dialysis occurred in 1977. This was attributed to intrinsic and occult endotoxin contamination of dialysis solution. Suspected provocative batches of peritoneal dialysate had endotoxin levels in the range of 2 to 2.5 endotoxin units (EU)/mL. See, for example, Karanicolas S, Oreopoulos DG, Izatt SH, et al: Epidemic of aseptic peritonitis caused by endotoxin during chronic peritoneal dialysis, N Engl J Med 1977;296:1336-7. A similar epidemic of aseptic peritonitis caused by endotoxin contamination in continuous cycling peritoneal dialysis patients was reported in 1998. See, for example, Mangram AJ, Archbald LK, Hupert M, et al: Outbreak of sterile peritonitis among continuous cycling peritoneal dialysis patients, Kidney Int 1988;54:1367-71. Other reported causes of aseptic peritonitis include intraperitoneal administered vancomycin (See, for example, Smith T, Baile G, Eisele G: Chemical peritonitis associated with intraperitoneal vancomycin, Ann Pharm 1991;25:602-3, and Chancy DI, Gouse SF: Chemical peritonitis secondary to intraperitoneal vancomycin, Am J Kidney Dis 1991;17:76-9), amphotericin B (See, for example, Benevent D, El Akoun N, Lagarde C: Dangers of administration of intraperitoneal amphotericin B in continuous ambulatory peritoneal dialysis, Press Med 1984;13:1844), and acetaldehyde (See, for example, Tuncer M, Sarikaya M, Sezer T, et al: Chemical peritonitis associated with high dialysate acetaldehyde concentrations, Nephrol Dial Transplant 2000;15:2037-40). A unique form of aseptic peritonitis, eosinophilic peritonitis, is a much more common entity that can occur shortly after the start of peritoneal dialysis. See, for example, Gokal R, Ramos JM, Ward MK, et al: 'Eosinophilic peritonitis' in CARD, Clin Nephrol 1981;15:328-330. As previously discussed, glucose polymers, such as icodextrin, can be used in place of dextrose in peritoneal dialysis solutions. Icodextrin is a polymer of glucose derived from the hydrolysis of corn starch. It has a molecular weight of 12-20,000 Daltons. Peritoneal dialysis solutions containing icodextrin as the osmotic agent are, in general, used for long dwell (4hour) exchanges. The majority of glucose molecules in icodextrin are linearly linked with a (1-4) glucosidic bonds (90%) while a small fraction (10%) is linked by a (1-6) bonds. Icodextrin was introduced into clinical practice in the= United Kingdom in 1994 and in other European countries beginning in 1996. Th.e clinical advantages of icodextrin for long dwells, especially in patients with high and high average transport status and loss of ultrafiltration, is well-accepted and contributed to its global popularity. See, for example, Wilkie ME, Plant MJ, Edwards L, et al: Icodextrin 7.5% dialysate solution (glucose polymer) in patients with ultrafiltration failure: extension of technique survival, Perit Dial Int 1997;17:84-7; Wolfson 2VI, Piraino B, Hamburger PJ, Morton AR, for the Icodextrin Study Group: A randomized controlled trial to evaluate the efficacy and safety of icodextrin in peritoneal dialysis, Am J Kidney Dis 2002;40:1055-65; and Mujais S, Nolph K, Gokal R, et al: Evaluation and management of ultrafiltration problems in peritoneal dialysis, Perit Dial Int 2000;20(Suppl 4):S5-S21. Since the introduction of icodextrin for use in peritoneal dialysis solutions, sporadic cases of aseptic peritonitis have been reported. See, for example, Pinerolo MC, Porri MT, D'Amico G: Recurrent sterile peritonitis at onset of treatment with icodextrin, Perit Dial Int 1999;19:491-2; Williams PF: Timely initiation of dialysis. Am J Kidney Dis 34:594-595, 1999; Williams PF, Foggensteiner L: Sterile/allergic peritonitis with icodextrin in CAPD patients, Perit Dial Int 2002;22:89-90; Foggensteiner L, Bayliss J, Moss H, et al: Timely initiation of dialysis - single-exchange experiences in 39 patients starting peritoneal, dialysis, Perit Dial Int 2002;22:471-6; Heering P, Brause M, Plum J, et al: Peritoneal reaction to icodextrin in a female patient on CAPD. Perit Dial Int 2001 ;21:321-2; Del Rosso G, Di Liberate L, Pirilli A, et al: A new form of acute adverse reaction to icodextrin in peritoneal dialysis patient, Nephrol Dial Transplant 2000;15:927-S; Goffin E, Scheiff JM: Transient sterile chemical peritonitis in a CAPD patient using icodextrin, Perit Dial Int 2002;22:90-1; Tintillier M, Pochet JM, Christophe XL, Scheiff JM, et al: Transient sterile chemical peritonitis with icodextrin: clinical presentation, prevalence, and literature review, Perit Dial Int 2002;22:534-7; and Gokal R: Icodextrin-associated sterile peritonitis, Perit Dial Int 2002;22:445-8. These patients typically presented with cloudy dialysate, no abdominal pain, and dialysate cell counts varying from 300 to 3500/mm3, with variable percentages of neutrophils, lymphocytes, and macrophages. In general, there is no change in ultrafiltration profile or peritoneal permeability for solutes. Cultures were invariably negative with no evidence of peritoneal or peripheral blood eosinophilia. Moreover, all solution components and endotoxin levels fell within the product specifications, and the icodextrin-based peritoneal dialysis solutions met all current Pharmacopoeia standards. Prompted by these reports, in 2001, the manufacturer of the icodextrin-containing solution (BAXTER HEALTHCARE CORPORATION) modified the Summary of Product Characteristics (SPC) to include cloudy effluent as an "undesirable side effect" of icodextrin. Parenteral pharmaceutical products are required to be free of contaminating substances, such as substances that can cause fever. Because endotoxins derived from gram-negative bacteria are the most common contaminant in parenteral products, the historic pyrogens of concern are LPS. Current Pharmacopeia standards are that one of two tests for pyrogenic contamination is applied to parenteral products. These tests are the rabbit pyrogen test and the LAL assay. Although generally reliable, both tests have shortcomings. The rabbit test relies on a febrile response that in turn depends upon the elaboration of pyrogenic cytokines. The rabbit pyrogen testing may be falsely negative, if the pyrogen is at a concentration too low to induce a systemic response, but of sufficient magnitude to produce a local inflammatory reaction. In turn, the more sensitive LAL test does not detect pyrogens other than LPS. Pyrogens, like viruses, fungi, DNA, gram-positive exotoxins, or bacterial cell wall components from gram positive bacteria, such as peptidoglycan and the like, will not be detected by the LAL test. See, for example, Dinarello CA, O'Conner JV, LoPreste G: Human leukocyte pyrogen test for detection of pyrogenic material in growth hormone produced by recombinant Escherichia coli, J Clin Microbiol 19S4;20:323-9; Poole S, Thorpe R, Meager A, et al: Detection of pyrogen by cytokine release, Lancet 1988;1(8577):130; Ray A, Redhead K, Selkirk S, et al: Variability in LPS composition, antigenicity and reactogenicity of phase variants of Bordetella pertussis, FEMS Microbiol Lett 1991 ;63:211-7; Taktak YS, Selkirk S, Bristow AF, et al: Assay of pyrogens by interleukm-6 release from monocytic cell lines, JPharm Pharmacol 1991;43:578-82; and Fennrich S, Fischer M, Hartung T, et al: Detection of endotoxins and other pyrogens using human whole blood, DevBiol Stand 1999;101:131-9. The global outbreak of aseptic peritonitis observed with, icodextrin-based peritoneal dialysis solutions as discussed above serves as a sentinel example of how contemporary parenteral products with microbial, non-endotoxin contaminants may be considered safe under Pharmacopoeia standards but provoke adverse clinical effects. Therefore, a need exists to provide improved standards for parenteral products that employ detection procedures to better ensure that the parenteral products are effectively free of contaminating substances. SUMMARY OF THE INVENTION The present invention generally relates to the detection of gram positive microbial contaminants. In particular, the present invention relates to methods and compositions that employ the detection of peptidoglycan in peritoneal dialysis solutions. The inventors have surprisingly discovered a novel cause of aseptic peritonitis-aseptic peritonitis associated with gram positive microbial contamination of a dialysis solution. Peptidoglycan is a major component of a gram, positive bacterial cell wall and thus can serve as a marker for gram positive bacteria. Thus, testing for peptidoglycans can be utilized to effectively prevent peritonitis in pa-tients that use the peritoneal dialysis solutions, such as peritoneal dialysis solutions that contain a glucose polymer including an icodextrin and the like. Icodextrin is derived from corn starch., a natural product. It is well known that products of natural origin are contaminated with a wide variety of micro-organisms. The inventors have found that some natural products, such as com starch, contain an acidophilic thermophilic bacteria, such as Alicyclobacillus acidocaldariuos. The later organism is ubiquitous in the food industry, particularly in acidic beverages. It is the alicyclobacillus that produces guaiacol, which is a causative substance for an 'off flavour orange juice. See, for example, Matsubara H, Goto K, Ma-tsumara T, et al. Alicyclobacillus acidiphilus sp. Nov., a novel thermo-acidophilic, omega-alicyclic fatty acid-containing bacterium isolated from acidic beverages. Int J Syst Evol Microbiol 2002; 52:1681-5. Peritoneal dialysis solutions and parenteral solutions in general have not been recognized to have contaminated by this organism or its degradation products. This is mainly because the current testing procedure for microbial contamination of peritoneal dialysis solutions and parenteral solutions in general are not capable of detecting this organism or its degradation products. To this end, in an embodiment, the present invention provides a method for manufacturing a peritoneal dialysis solution. The method includes providing a glucose polymer-based solution; adding a reagent to the glucose polymer-based solution wherein the reagent is capable of reacting with a peptidoglycan; deterrnining an amount of the peptidoglycan using the reagent; and using the glucose polymer-based solution to provide the peritoneal dialysis solution if it is determined that a sufficiently low level of the peptidoglycan is present. In an embodiment, the reaction initiates a serine protease cascade. In an embodiment, the serine protease cascade includes a prophenol oxidase cascade. m an embodiment, the reagent is derived from a silkworm larvae plasma. Li an embodiment, the amount of peptidoglycan is further determined by a colorimetric measurement in response to the reaction between the peptidoglycan and the reagent. In an embodiment, the sufficiently low level of the peptidoglycan is about 10 ng/mL or less. In an embodiment, the glucose polymer-based solution includes an Icodextrin. In an embodiment, the reagent is added to the icodextrin in a raw material form that is used to make the glucose polymer-based solution. In another embodiment, the present invention provides a method of providing peritoneal dialysis to a patient. The method includes preparing a peritoneal dialysis solution utilizing a reagent to ensure that the peritoneal dialysis solution has a sufficiently low level of a peptidoglycan so as to prevent peritonitis in the patient; and providing the peritoneal dialysis solution to the patient. hi an embodiment, the peritoneal dialysis solution includes an icolextrin-based solution. hi an embodiment, the peritoneal dialysis includes an automated peritoneal dialysis, a continuous ambulatory peritoneal dialysis and the like. In an embodiment, the patient is monitored for peritonitis during peritoneal dialysis. For example, a dialysis effluent can be collected from the patient to determine an IL-6 response that correlates to an incidence of peritonitis. In an embodiment, the reagent is used to determine if the amount of the peptidoglycan exceeds about 10 ng/mL in the peritoneal dialysis solution prior to use during peritoneal dialysis. In yet another embodiment, the present invention provides a method of testing a peritoneal dialysis solution for an amount of a peptidoglycan that exceeds a level sufficient to cause peritonitis. The method includes adding a reagent to the peritoneal dialysis solution wherein the reagent is capable of reacting with the peptidoglycan to initiate a serine protease cascade; and determining the amount of the peptidoglycan. For example, the icodextrin-based solution can be tested to determine if the amount of peptidoglycan exceeds about 10 ng/mL. hi still yet another embodiment, the present invention provides an icodextrin composition that includes a reagent capable of reacting with a peptidoglycan. . In an embodiment, a level of peptidoglycan can be established above which the product would produce sterile peritonitis. In an embodiment, use of affinity columns with resins that bind peptidoglycan can be used to minimize the contamination of peptidoglycan in glucose polymers. An advantage of the present invention is to provide improved peritoneal dialysis solutions. Another advantage of the present invention is to provide improved methods for manufacturing and using peritoneal dialysis solutions that employ a detection protocol to determine the presence of peptidoglycan in the peritoneal dialysis solution. Yet another advantage of the present invention is to provide improved testing procedures that can be employed to prevent peritonitis in patients that receive peritoneal dialysis therapy. Yet still another advantage of the present invention is to provide an improved icodextrin composition that utilizes a detection procedure in the manufacture thereof to determine the presence of peptidoglycan. Additional features and advantages of the present invention are described in, and will be apparent from, the following Detailed Description of the Invention and the figures. BRIEF DESCRIPTION OF THE FIGURES Figure 1 illustrates a correlation between IL-6 response in a PBMC assay and peptidoglycan concentration in icodextrin. IL-6 response was measured in freshly isolated monocytes from healthy volunteers. Each symbol and line represent data from a single donor. Figure 2 illustrates an effect of peptidoglycan on the infiltration of neutrophils in the peritoneal fluid of rats. Peritoneal fluid was collected six hours after single injection (35 mL/kg) of icodextrin containing peptidoglycan. Figure 3 illustrates an effect of peptidoglycan on TNF-a in the peritoneal fluid ofrats. Figure 4. illustrates an effect of peptidoglycan on IL-6 in the peritoneal fluid of rats. Figure 5 illustrates frequency (%) of aseptic peritonitis reported with use of icodextrin. DETAILED DESCRIPTION OF THE INVENTION The present invention generally relates to the detection of gram positive organisms and fragments thereof. In particular, the present invention relates to methods and compositions that employ the detection of peptidoglycan. in peritoneal dialysis solutions. The inventors have surprisingly discovered a novel cause of aseptic peritonitis-aseptic peritonitis associated with gram positive microbial contamination of a dialysis solution. Peptidoglycan is a major component of a gram positive bacterial cell wall and thus can serve as a marker for gram positive bacteria. In this regard, testing for peptidoglycans can be utilized to effectively prevent peritonitis in patients that use the peritoneal dialysis solutions, such as peritoneal dialysis solutions that contain a glucose polymer including an icodextrin and the like. Aseptic peritonitis associated with icodextrin-based peritoneal dialysis solutions is believed to be the largest adverse event reported for a peritoneal dialysis solution due to a contaminant of microbial origin. Based on the experimental investigations as described in detail below, this suggests that peptidoglycan in the icodextrin-based peritoneal dialysis solution was the causative agent of aseptic peritonitis. Further, pharmacovigilence data as detailed below supports the effectiveness of the corrective action and manufacturing screening procedure to prevent the occurrence of peritonitis. These findings illustrate that while endotoxin is deservedly one of the more worrisome bacterial product that can cause adverse effects to patients, it is not the sole one. In this regard, non-endotoxin pyrogens, such as peptidoglycans, that have not been previously identified, are capable of producing clinically significant inflammation. Thus, this demonstrates that parenteral pharmaceutical products that pass the compendial tests and so meet Pharmacopoeia standards may still require a further level of testing to effectively determine the efficacy and safe use of such products to better ensure quality of life issues associated with use of same. In the present invention, non-LPS pyrogen contamination was recognized as a problem because peritoneal dialysis exchanges permitted the direct observation of peptidoglycan-induced inflammation in situ. Peptidoglycan is a heteropolymer formed from /3 (1-4) linked N-acetylmuramic acid and N-acetyl-D-glucosamine residues crosslinked by peptide bridges. See, for example, Royce CL, Pardy RL: Endotoxin-Iike properties of an extract from a symbiotic, eukaryotic cholerella-like green algae, J Endotoxin Res 1996;3:437-44. The glycan backbone is chemically homogenous, whereas the peptides cross-linking the sugars vary. Peptidoglycan occupies approximately 40% by weight of gram positive cell wall, but about 1-10% of the total weight of the gram negative cell walls. Royce CL, Pardy RL: Endotoxin-like properties of an extract from a symbiotic, eukaryotic cholerella-like green algae, J Endotoxin Res 1996;3:437-44. Peptidoglycan and another cell wall constituent, lipoteichoic acid, include virtually all of the major inflammatory inducing components of gram-positive cellular walls. See, for example, Sriskandan S, Cohen J: Gram-positive sepsis, In: Opal SM, Cross AS, eds. Bacterial Sepsis and Septic Shock, Philadelphia: W. B. Saunders Company, 1999:397-412. Like endotoxins, peptidoglycans can induce cytokine production in a wide variety of cells and have long been recognized to have immunomodulatory actions. See, for example, Gamer RE, Hudson JA: Intravenous injection of Candida-derived mannan results in elevated tumor necrosis factor alpha levels in serum, Infect Immun 1996;64:4561-6; and Schwab J: Phlogistic properties of peptidoglycan-polysaccharide polymers from cell walls of pathogenic and normal flora bacteria which colonize humans, Infect Immun 1993;61:4535-9. However, peptidoglycans are several orders of magnitude less potent than endotoxins as provocateurs of these biological effects. See, for example, Henderson B, Poole S, Wilson M: Bacterial modulins: a novel class of virulence factors which cause host tissue pathology by inducing cytokine synthesis, Microbiol Rev 1996;60:316-41; and Nakagawa Y, Maeda H, Murai T: Evaluation of the in vitro pyrogeri test system based on proinflammatory cytokine release from human monocytes: Comparison with a human whole blood culture test system and with the rabbit pyrogen test, Clin DiagLab Immunol 2002;9:588-97. For example, the minimum pyrogenic dose of peptidoglycans in rabbits is 7.3 fig/kg, while that of endotoxins is 0.0027 /tg/kg. See, for example, Henderson B, Poole S, Wilson M: Bacterial modulins: a novel class of virulence factors which cause host tissue pathology by inducing cytokine synthesis, Microbiol Rev 1996;60:316-41. In addition to the absence of pyrogenic containing substances, safety of parenteral products are generally defined by Pharmacopoeia tests to determine their sterility. Bacterial cultures are generally performed at neutral pH using an incubation temperature between 20-35°C. These are suboptimal conditions for the growth of thermophilic, acidophilic microorganisms such as Alicyclobacittus acidocaldarius that require an acid medium and elevated temperature for growth. Therefore, routinely employed "sterility definitions" and the supporting assays may fail to detect microorganisms that do not grow under conventional conditions. In an embodiment of the present application, acid hydrolysis at an elevated temperature is used for hydrolysis of starch to produce icodextrin. These manufacturing conditions are suitable for the growth of Alicycclobacittus acidocadarius, but discordant with those used to determine sterility based on bioburden. As referenced above, a detailed description of the investigative findings are provided below in accordance with an embodiment of the present invention by way of example and without limitation: CHEMICAL AND PHYSICAL INVESTIGATIONS The majority of glucose molecules in icodextrin are linearly linked with a (1-4) glucosidic bonds (90%), while a small fraction (10%) are linked by a (1-6) bonds. Molecular weight distribution of icodextrin was performed by gel permeation chromatography. The distribution of o(l- 6 ) and o(l- 4) glucosidic links in icodextrin was assessed by nuclear magnetic resonance spectroscopy. Volatile and semi-volatile organic impurities were examined by high performance liquid chromatography and mass spectroscopy. DIALYSATE EFFLUENT ANALYSIS Dialysate effluent samples from patients were analyzed for icodextrin metabolites, triglycerides, total protein and selective pyrogenic cytokines (JJL-6, EL-1/3 and TNF-a). Icodextrin metabolites were assayed Using high performance anion exchange chromatography with pulsed amperometric detection. See, for example, Burke RA, Hvizd MG, Shockley TR: Direct determination of polyglucose metabolites in plasma using anion-exchange chromatography with pulsed amperometric detection, J Chromatogr B 1997;693:353-7. Triglyceride and protein analysis were performed with Boehringer Mannheim/Hitachi 911 Chemistry analyzer. Cytokine measurements were made using ELISA kits (R&D Systems, Minneapolis, MM). MEASUREMENT OF PYROGENS Endotoxin concentration in icodextrin solution was determined by a fixed point chromogenic LAL test. See, for example, Weary M, Dubczak J, Wiggins J, et al: Validating an LAL chromogenic substrate pyrogen test for large volume parenterals, In: Watson SW, Levin J, Novitsky TJ, eds, Detection of bacterial endotoxin with limulus amebocyte lysate test. New York: Alan R. Liss, 1987:307-22. Rabbit pyrogen test was performed in accordance with the guidelines provided in the European Pharmacopeia. European Pharmacopoeia, Pyrogens, 4th ed. Strasbourg, France: Council of Europe, 2002:131-2. An ex vivo pyrogen test that measures IL-6 response in freshly isolated peripheral blood mononuclear cells (PBMC) following exposure to a test substance was used to quantitate non-endotoxin pyrogens. See, for example, Dinarello CA, O'Conner JV, LoPreste G: Human leukocyte pyrogen test for detection of pyrogenic material in growth hormone produced by recombinant Escherichia coli, J Clin Microbiol 1984;20:323-9; and Poole S, Thorpe R, Meager A, et al: Detection of pyrogen by cytokine release, Lancet 1988; 1 (8577): 130. MEASUREMENT OF PEPTIDOGLYCANS Peptidoglycan (PG) quantitation was performed with the silkworm larvae plasma (SLP) test (Wako Pure Chemical Industries, Ltd., Osaka, Japan). See, for example, Tsuchiya M, Asahi N, Suzouki F: Detection of peptidoglycan and B-glucan with silkworm larvae plasma test, FEMS Immunol Medical Micrbiol 1996;15:129-34; and U.S. Patent No. 4,970,152. SLP contains all the factors of the prophenol oxidase (PPO) cascade, a self-defense mechanism of insects. The PPO cascade is initiated by peptidoglycan, in which PPO is ultimately activated to phenol oxidase. The phenol oxidase activity is colorimetrically detected with 3,4-dihydroxyphenylalanine as a substrate. The limit of detection of peptidoglycan in icodextrin solution was found to be 7.4 ng/mL. The SLP test does not detect endotoxins. As fully disclosed in U.S. Patent No. 4,970,152, for example, the detection of peptidoglycan (or (3-G) can be carried out as follows. A sample containing the peptidoglycan is well mixed with a reagent that includes a fraction which specifically reacts with peptidoglycan ("PG") to prepare a reaction solution. After a certain period of time, an enzymatic activity, e.g., activity of BAEEase, PPAE, PO, etc., in the reaction solution can be measured by a conventional method and compared with calibration curves previously obtained by using PG standard solutions with known concentrations to determine the amount of PG. Alternatively, it is possible to apply a phenomenon that a time required for the activation of PO depends on the concentration of PG in the sample. That is, after mixing the PG reagent with a sample in the presence of the substrate of PO, a time required for reaching a certain value of the amount of reaction product generated by PO is measured. By way of example and not limitation, an experimental procedure that utilizes the SLP test can be conducted in accordance with an embodiment of the present invention as follows. Peptidoglycan (PG) and (1,3)—D-glucan (BG) are components of the cell walls of gram positive bacteria and fungi, respectively. PG and BG are measured with the Silkworm Larvae Plasma (SLP) test. The SLP test contains all the factors of the pro-phenol oxidase (PPO) cascade, an important self-defense mechanism of insects. The PPO cascade is initiated by peptidoglycan, in which PPO converts 3,4-dihydroxyphenylalanine (DOPA) to melanin. The resulting formation of melanin is colorimetrically detected at 650 nm using a standard plate reader. The raw material icodextrin is tested undiluted and has a limit of detection (LOD) of 0.74 ng/ml (the lowest detectable standard point). The finished product, such as EXTRANEAL, is tested after diluting tenfold in order to mitigate the matrix inhibition caused by the presence of electrolytes. The sample dilution step results in a LOD of 7.4 ng/ml after correcting for the 1:10 dilution. ANIMAL STUDIES No Observed Effect Level (NOEL) for peptidoglycan in icodextrin was determined in a rat model. A total of 45 male Sprague-Dawley rats (Harlan Inc; Indianapolis, IN, USA), weighing 255-280 g were divided into 9 equal groups. Each group received a single intraperitoneal injection of icodextrin spiked with 0, 1, 5, 10, 50, 100, 500, 1000 or 5000 ng/mL peptidoglycan at a dose of 35 mL/kg. Peptidoglycan derived from Staphylococcus aureus (Toxin Technology Inc., Sarasota, FL, USA) was used in these experiments. Six hours post injection, the rats were sacrificed, and the fluid in the peritoneal cavity was quantitatively collected by determining the weight and volume. Peritoneal fluid was analyzed for nucleated cell counts and differential counts, total protein, "and IL-6 and TNF-a concentrations. STATISTICAL ANALYSIS Post market surveillance data on several hundred batches of icodextrin manufactured between July 2000 and September 2002 were analyzed to determine an association between peptidoglycan level and the incidence of aseptic peritonitis. To accumulate sufficient complaint frequencies to effectively display complaints per million (CPM), data were classified into peptidoglycan level in a log scale, namely, 3A, 7.4-15, 15-30, 30-60, and =60 ng/mL. For each of peptidoglycan concentration range, the total complaints and the total units sold were calculated. The CPM units sold were computed as the total complaints divided by the total units sold multiplied by one million. Negative binomial regression was used to assess the association between CPM and peptidoglycan level. The statistical analysis was performed using the SAS procedure GENMOD (SAS Institute, Gary, NC, USA). CLINICAL CASES According to reports received through the BAXTER HEALTHCARE CORPORATION'S global pharmacovigilance system in 2000, the frequency [(number of complaints number of patients treated) x 100] of aseptic peritonitis was 0.095%. There was a steady increase in reported cases in 2001 to a peak frequency of 1.04% in March 2002. The patients were rarely febrile or toxic in appearance; abdominal pain was modest to absent; the dialysate was cloudy and cellular with dialysate cell counts varying from 300 to 3500/mm3 (variable percentages of neutrophils, lymphocytes, and macrophages without eosinophils). Unlike bacterial peritonitis, there was no change in ultrafiltration or peritoneal permeability for small solutes. Blood and dialysate cultures were invariably negative. Antibiotics were variably instituted by the local physicians. All clinical signs resolved upon stopping icodextrin. hi some cases, icodextrin was restarted, and aseptic peritonitis recurred. BAXTER HEALTHCARE CORPORATION initiated a voluntary worldwide recall of several hundred batches of icodextrin in May 2002. CHEMICAL AND PHYSICAL INVESTIGATIONS OF ICODEXTRIN Extensive chemical and physical investigations of recalled icodextrin batches were performed. These analyses did not reveal any differences in molecular weight distribution of icodextrin, percent branching of glucosidic bonds, or trace volatile and semi-volatile organic impurities between the batches associated with aseptic peritonitis and those not associated with adverse clinical events. All solution components of complaint batches of icodextrin-containing dialysate were within the product specifications and met current Pharmacopoeia standards. DIALYSATE EFFLUENT ANALYSIS A marked elevation in IL-6 concentration was observed in the dialysate effluent from a patient with aseptic peritonitis compared to control effluent (>5000 versus 59 pg/mL, respectively). An increase in protein concentration was noted with the complaint sample compared to the control (236 mg/dL versus 125 mg/dL, respectively). There was no difference in icodextrin and its metabolites (glucose polymers with degree of polymerization from 2 to 7) between the complaint and control samples. These results indicated that neither icodextrin nor its metabolites were the likely cause of aseptic peritonitis. PYROGEN ANALYSIS OF ICODEXTRIN Endotoxin levels in all the icodextrin samples associated with aseptic peritonitis were found to be within the product limit ( dialysate batches and the icodextrin raw material used to manufacture the complaint batches of peritoneal dialysate as illustrated in Table 1 below: Tablel: IL-6 response of complaint and non-complaint batches of icodextrin in the PBMC assay. In this assay, an IL-6 response of greater than 500 pg/mL is considered a positive pyrogenic response. (Table Removed) "Eagle minimum essential medium with supplemental components, 'Baxter experimental product, °Glucose containing standard peritoneal dialysis solution The IL-6 provoking substance in the complaint samples was unaffected in the presence of polymyxin B, thus suggesting that it was not LPS. See, for example, Pool EJ, Johaar G, James S, et al: Differentiation between endotoxin and non-endotoxin pyrogens in human albumin solutions using an ex vivo whole blood culture assay, J Immunoassay 1999;20:79-89. In a filtration experiment using a 30 kD molecular weight cut-off filter, the contaminant producing the inflammatory response in the PBMC assay was found in the retentate, suggesting the molecular weight of the substance was >30 kD, i.e. larger than icodextrin. The negative assays for LPS, but positive PBMC IL-6 response indicated that the likely cause of aseptic peritonitis was a non-endotoxin, pyrogen contaminant in icodextrin raw material used to manufacture the final peritoneal dialysis solution. PEPTIDOGLYCAN AND MICROBIOLOGICAL ANALYSIS Analysis of several hundred recalled batches of icodextrin indicated that 41% of the batches were contaminated with peptidoglycan that was detected by the SLP assay. Peptidoglycan concentrations ranged from the detection limit of 7.4 ng/mL to 303 ng/mL. Because the manufacture of icodextrin from maltodextrin requires heat and acidification, a microbiological investigation for the presence of fastidious organisms was undertaken. Early steps of icodextrin were found to be contaminated with a thefmophilic, acidiophilic, gram positive organism, Alicydobacillus acidocaldaritis. Alicydobacillus was the source of the contaminating peptidoglycan. Heat and sterile filtration procedures applied to the near final product eliminated the bacteria, but not the peptidogycan contaminants. A positive correlation was found between peptidoglycan levels in icodextrin and the IL-6 response observed in the PBMC assay (See, Fig.l). Substantial variability in the IL-6 response was seen between donors suggesting a range of sensitivities to peptidoglycan. ANIMAL STUDIES The effects of intraperitoneal administration of peptidoglycan in rats was investigated in order to establish a NOEL. This can be used to establish a regulatory specification for icodextrin manufacturing. Total protein, white blood cells and neutrophils were elevated in the peritoneal fluid of icodextrin + peptidoglycan-treated rats compared to control rats that received icodextrin without peptidoglycan. Infiltration of neutrophils in peritoneal fluid showed a dose dependent increase with a NOEL at 100 ng/mL (See, Fig.2). Both inflammatory cytokines showed dose dependent increases with NOEL values at 10 ng/mL for TNF-a (See, Fig.3) and 100 ng/mL for IL-6 (See, Fig.4). The lowest NOEL for peptidoglycan was for TNF-a response which was 10 ng/mL. CORRELATION BETWEEN PEPTIDOGLYCAN AND ASEPTIC PERITONITIS A positive correlation was found between peptidoglycan concentration in icodextrin and CPM as illustrated in Table 2 below: Table 2: Correlation between Complaints Per Million (CPM) units sold and peptidoglycan concentration in icodextrin solution (Table Removed) Complaints Per Million (CPM) units sold was computed as the total complaints divided by the total units sold multiplied by one million. The baseline CPM was 18.2, when peptidoglycan levels were below the detection limit of 7.4 ng/mL. In contrast, the CPM was 252.9, when peptidoglycan levels were equal to or greater than 60 ng/mL. The association between CPM and peptidoglycan was highly significant (pO.OOOl). INCIDENCE OF ASEPTIC PERITONITIS FOLLOWING CORRECTIVE ACTION In May 2002, BAXTER HEALTHCARE CORPORATION recalled all batches of icodextrin contaminated with peptidoglycan at a concentration >10 ng/mL, as well as all lots that were not assayed for peptidoglycan at the time of the recall. Li addition, an internal regulatory specification for peptidoglycan below the detection limit of the assay ( Fig. 5 shows the incidence rate of aseptic peritonitis by month beginning September 2001 to January 2003. The frequency of complaints has decreased from a peak value of 1.04% in March 2002 to 0.013% hi January 2003 following the implementation of corrective actions. The number of patients using a commercially* available peritoneal dialysis solution known as EXTRANEAL from BAXTER HEALTHCARE CORPORATION during this period remained at approximately 7,000. These results suggest that corrective actions have been effective in preventing excess complaints of aseptic peritonitis due to peptidoglycan contamination in icodextrin-containing dialysis solution. As previously discussed, the present invention relates to methods and compositions that employ the detection of peptidoglycan in peritoneal dialysis solutions. This allows testing for bacterial fragments as peptidoglycans are the majorcell wall component of gram positive organisms. In this regard, peptidoglycan detection can be effectively utilized to prevent peritonitis in patients that use the peritoneal dialysis solutions, such as peritoneal dialysis solutions that contain a glucose polymer including icodextrin and the like. It should be appreciated that compositions, peritoneal dialysis solutions and methods of manufacturing and using same can be provided hi any suitable manner in accordance with an embodiment of the present invention. In an embodiment, the present invention provides bioburden testing, such as bioburden testing for acidophilic thermophilic organisms according to standard procedures as described in various Pharmacopoeias. This type of testing can be utilized as an added level of testing in addition to the testing for bacterial fragments by detection of peptidoglycans as previously discussed. Li an embodiment, the present invention provides methods for manufacturing a peritoneal dialysis solution. The method can include any suitable number and type of processing stages. For example, the process includes providing a glucose polymer; adding a reagent to the glucose polymer wherein the reagent is capable of reacting with a peptidoglycan; determining an amount of the peptidoglycan; and using the glucose polymer to make the peritoneal dialysis solution if it is determined that a sufficiently low level of the peptidoglycan is present in the glucose polymer. If the amount of peptidoglycan or the like exceeds this level, such as about 10 ng/mL or less, the glucose polymer can be further processed to remove the peptidoglycan or the like in order to achieve a sufficiently low level of same. The glucose polymer can be further processed in any suitable manner. In an embodiment, the glucose polymer can be processed with any suitable number and type of separation devices, such as an affinity device and/or the like. In an embodiment, the present invention provides compositions, such as glucose polymer compositions that can be used to prepare peritoneal dialysis solutions. A variety of different and type of compositions and solutions containing same can be utilized. For example, the type of compositions and solutions can same can be found in U.S. Patent No. 4,761,237, entitled 'TERITONEAL DIALYSIS SOLUTION CONTAINING CARBOHYDRATE POLYMERS; U.S. Patent No. 4,886,789, entitled "PERITONEAL DIALYSIS AND COMPOSITIONS FOR USE THEREIN"; U.S. Patent No. 6,077,836, entitled "PERITONEAL DIALYSIS AND COMPOSITIONS FOR USE THEREIN"; AND U.S. Patent No. 6,248,726 Bl, entitled "METHOD OF PERITONEAL DIALYSIS USING GLUCOSE POLYMER SOLUTIONS, the disclosures of which in their entirety are incorporated herein by reference. Additional examples of compositions and solutions containing same can be can be found in U.S. Patent Application No.10/327,264, entitled BIOCOMPATTBLE DIALYSIS FLUIDS CONTAINING ICODEXTRINS, filed on December 20, 2002; and U.S. Patent Application No. 09/206,063, entitled PERITONEAL DIALYSIS SOLUTION CONTAINING MODIFIED ICODEXTRINS, filed on December 4, 1998, the disclosures of which in their entirety are incorporated herein by reference. In an embodiment, the peritoneal dialysis solutions can include EXTRANEAL by BAXTER HEALTHCARE CORPORATION or suitable modifications thereof. hi an embodiment, the present invention includes methods of providing peritoneal dialysis, such as continuous ambulatory peritoneal dialysis and automated peritoneal dialysis. In continuous ambulatory peritoneal dialysis, the patient performs several drain, fill, and dwell cycles during the day, for example, about four times per day. Each treatment cycle, which includes a drain, fill and dwell, takes about four hours. Automated peritoneal dialysis is similar to continuous ambulatory peritoneal dialysis in that the dialysis treatment includes a drain, fill, and dwell cycle. However, a dialysis machine automatically performs three or more cycles of peritoneal dialysis treatment, typically overnight while the patient sleeps. With automated peritoneal dialysis, an automated dialysis machine fluidly connects to an implanted catheter or the like. The automated dialysis machine also fluidly connects to a source or bag of fresh dialysis solution and to a fluid drain. The dialysis machine pumps spent dialysis solution from the peritoneal cavity, through the catheter, to the drain. The dialysis machine then pumps fresh dialysis solution from the source, through the catheter, and into the patient's peritoneal cavity. The automated machine allows the dialysis solution to dwell within the cavity so that the transfer of waste, toxins and excess water from the patient's bloodstream to the dialysis solution can take place. A computer controls the automated dialysis machine so that the dialysis treatment occurs automatically when the patient is connected to the dialysis machine, for example, when the patient sleeps. In this regard, the dialysis system automatically and sequentially pumps fluid into the peritoneal cavity, allows for dwell, pumps fluid out of the peritoneal cavity, and repeats the procedure. Several drain, fill, and dwell cycles will occur during the treatment. Also, a final volume "last fill" is typically used at the end of the automated dialysis treatment, which remains in the peritoneal cavity of the patient when the patient disconnects from the dialysis machine for the day. Automated peritoneal dialysis frees the patient from having to manually perform the drain, dwell, and fill steps during the day. hi an embodiment, automated peritoneal dialysis can be performed by utilizing an admix device, such as ADMIX HOMECHOICE by BAXTER HEALTHCARE CORPORATION or suitable modifications thereof. In an embodiment, the present invention provides a test to determine if a peritoneal dialysis solution, such as an icodextrin-based solution, includes peptidoglycan that exceeds a level sufficient to cause peritonitis in the patient that uses same. The present invention provides a detection protocol that utilizes a reagent, such a reagent derived from a silkworm larvae plasma, for such purpose. It should be appreciated that the detection procedure can be carried out at any suitable stage prior to use of the peritoneal dialysis solution. For example, the reagent can be added to a glucose polymer composition, such as an icodextrin composition, in raw material form to determine the presence of peptidoglycan. If the level of peptidoglycan is at a sufficiently low level, the composition can then be utilized to prepare the peritoneal dialysis solution, hi another embodiment, the reagent can be added to the peritoneal dialysis solution, such as after the sterilization process in finished product form. For example, the reagent can be added to the peritoneal dialysis solution that is contained within any suitable solution bag, such as a single-chambered solution bag or a multi-chamber solution bag. An example of a multi-chamber solution bag or container is provided in U.S. Patent No. 5,431,496, the disclosure of which in its entirety is incorporated herein by reference. As described herein, all patent applications and publications including patent publications are incorporated herein by reference in their entirety. It should be understood that various changes and modifications to the presently preferred embodiments described herein will be apparent to those skilled in the art. i Such changes and modifications can be made without departing from the spirit and scope of the present invention and without diminishing its intended advantages. It is therefore intended that such changes and modifications be covered by the appended claims. WE CLAIM: 1. A method for manufacturing a peritoneal dialysis solution, the method comprising: providing a glucose polymer; performing a bioburden test on the glucose polymer in an acidic medium and at an elevated temperature to detect contaminating Alcyclobacillus acidocaldarius; testing the glucose polymer with a reagent derived from silkworm larvae plasma, wherein the reagent is reactive with any peptidoglycan in the glucose polymer to determine a peptidoglycan concentration; and using the glucose polymer to prepare the peritoneal dialysis solution if the peptidoglycan concentration is determined to be about 10 ng/mL or less. 2. The method as claimed in Claim 1 comprising testing the peritoneal dialysis solution with a reagent derived from silkworm larvae plasma, wherein the reagent is reactive with any peptidoglycan in the peritoneal dialysis solution to determine if the peptidoglycan concentration in the peritoneal dialysis solution is less than about 10 ng/mL or less. 3. The method as claimed in claim 1, wherein the reaction with the reagent initiates a serine protease cascade. 4. The method as claimed in claim 1, wherein the peptidoglycan concentration is determined by a colorimetric measurement. 5. The method as claimed in claim 1, wherein the glucose polymer includes icodextrin. 6. A method of testing a glucose polymer for peptidoglycan contamination, the method comprising: providing a glucose polymer; performing a bioburden test on the glucose polymer in an acidic medium and at an elevated temperature to detect Alcyclobacillus acidocaldarius, which is a source of peptidoglycan; and testing the glucose polymer with a reagent derived from silkworm larvae plasma, wherein the reagent is reactive with any peptidoglycan in the glucose polymer to determine a peptidoglycan concentration in the glucose polymer. 7. The method as claimed in claim 6, wherein the reaction with the reagent initiates a seine protease cascade. 8. The method as claimed in claim 6, wherein the serine protease cascade includes a prophenol oxidase cascade. 9. The method of claim 6, wherein the glucose polymer includes icodextrin.

Documents:

4010-DELNP-2006-Abstract-(13-04-2012).pdf

4010-delnp-2006-Abstract-(14-02-2014).pdf

4010-delnp-2006-abstract.pdf

4010-delnp-2006-assignments.pdf

4010-DELNP-2006-Claims-(13-04-2012).pdf

4010-delnp-2006-Claims-(14-02-2014).pdf

4010-DELNP-2006-Claims-(31-12-2009).pdf

4010-delnp-2006-claims.pdf

4010-DELNP-2006-Correspondence Others-(13-04-2012).pdf

4010-delnp-2006-Correspondence Others-(14-02-2014).pdf

4010-DELNP-2006-Correspondence Others-(24-01-2012).pdf

4010-delnp-2006-Correspondence Others-(25-02-2014).pdf

4010-delnp-2006-correspondence-others (09-12-2009).pdf

4010-delnp-2006-correspondence-others (26-02-2008).pdf

4010-DELNP-2006-Correspondence-Others-(09-12-2009).pdf

4010-DELNP-2006-Correspondence-Others-(31-12-2009).pdf

4010-delnp-2006-correspondence-others.pdf

4010-delnp-2006-description (complete).pdf

4010-DELNP-2006-Drawings-(13-04-2012).pdf

4010-delnp-2006-drawings.pdf

4010-DELNP-2006-Form-1-(13-04-2012).pdf

4010-delnp-2006-form-1.pdf

4010-delnp-2006-form-18 (26-02-2008).pdf

4010-DELNP-2006-Form-2-(13-04-2012).pdf

4010-delnp-2006-Form-2-(14-02-2014).pdf

4010-delnp-2006-form-2.pdf

4010-DELNP-2006-Form-3-(24-01-2012).pdf

4010-delnp-2006-form-3.pdf

4010-delnp-2006-form-5.pdf

4010-DELNP-2006-GPA-(13-04-2012).pdf

4010-delnp-2006-gpa.pdf

4010-delnp-2006-pct-101.pdf

4010-delnp-2006-pct-210.pdf

4010-delnp-2006-pct-220.pdf

4010-delnp-2006-pct-237.pdf

4010-delnp-2006-pct-304.pdf

4010-DELNP-2006-Petition-137-(24-01-2012).pdf