|Title of Invention
"CONTROLLED RELEASE MICROSPHERES"
|The present invention relates to controlled release microspheres comprising: biodegradable microspheres formed of from 85% to 99% by weight of polylactic-co-glycolic acid (PLGA) in a ratio of 50% lactic to 50% glycolic acid and, optionally, from 0% to 5% by weight of polyethylene glycol (PEG); and an antibiotic agent entrapped in said microspheres and capable of being eluted from said microspheres wherein the microspheres are from about 6 µm to about 20 µm in diameter.
|CROSS REFERENCE TO RELATED APPLICATIONS
This application claims priority of U.S. Provisional Application Serial No, 60/408,496, filed September 5, 2002 and U.S. Provisional Application Serial No. 60/408,502, filed September 5, 2002,
This invention relates generally to microspheres capable of time releasing a drug and, more particularly to microspheres for implantation, injection, or other placement totally or partially vvitliin the body that are capable of near-linear controlled release of an antibiotic for an extended period of time for the treatment and prevention of infections involving the body,
Historically, osteomyelitis treatment has consisted of debridement of infected tissues, irrigation with an antiseptic solution, and four to six weeks of parenteral antibiotic treatment. Due to poor penetration of the antibiotic into the infected bone site, high serum concentrations of the antibiotic need to be employed for extended periods of time in order to produce bactericidal levels within the bone tissue. These high serum levels can be associated with nephrotoxicity or ototoxicity, and can cause gastroinstestinal side effects. Due to the morbitiy associated with high serum levels of antibiotics, many local delivery methods have been described including bone cement with antibiotics, collagen sponge with geutamycin, polymeric carriers with various antibiotics, and calcium sulfate carriers of antibiotics.
The need for a local drug delivery system to deliver antibiotics directly to the infection site led many physicians to mix antibiotics and polymethyl methacryiate (PMMA) bone cement into bead.s and place these beads into the debrided bone defect. Typically, these beads have been
shown to deliver non-linear doses of antibiotic over the course of only a few weeks, and after the
antibiotic has been eluted, the cement beads must be removed, as the cement is not
biodegradable and may become a nidus for infection.
Infection may complicate any surgical treatment. Areas of high risk include fractures of
bone treated with metal rods, plates or external fixators. The risk is particularly high if the
fracture was open (compound fractures). Other surgical procedures are also at risk including
vascular bypass surgery with tire use of artificial graft material, general surgical procedures such
as hernia repair and various procedures performed about the uterus and bladder. Once
established, these infections are typically treated with surgical drainage and systemic antibiotics.
Just as in the treatment of osteomyelitis, the treatment for infection may be prolonged, costly
and may fail. There exists a need for a safe, effective local antibiotic delivery device that will
improve healing aird prevent complications.
The present invention is distinguished over the prior art in general, and these patents in
particular by biodegradable microspheres implanted, injected, or otherwise placed totally oi
partially witliin the body that are capable of near-linear controlled release of an antibiotic for a
predetermined period of time for the treatment and prevention of infections involving the body
The microspheres aie formed of polylactic-co-glycolic acid (PLGA) and an effective amount of
antibiotic sufficient to produce bactericidal levels in body tissues, and may or may not include
polyethylene glycol (PEG). The microspheres exhibit near-linear delivery of the antibiotic for at
least 4 weeks at levels exceeding the minimum inhibitory concentration (MIC) for organisms
commonly found to be die cause of infections. The microspheres allow antibiotics to be
delivered at the time of various surgical treatments to decrease the occurrence of infection, and
may be used for the treatment of open fractures, open reduction and internal fixation with
metallic fixation of fractures, placement of joint replacement devices, and placement of various
graft materials used in cardiovascular, general, gynecologic, and neurosurgical procedures.
DISCLOSURE OF THE INVENTION
It is therefore an object of the present invention to provide antibiotic microspheres for the treatment and prevention of infections that are capable of near-linear release of the antibiotic for an extended period of time, and at levels exceeding the minimum inliibitory concentration (MIC) for organisms commonly found to be the cause of infection,
It is another object of this invention to provide a biodegradable microsphere antibiotic delivery system for the treatment and prevention of infections and osteomyelitis that eliminates the need for an additional surgery to remove the drug carrier.
Another object of this invention is to provide antibiotic microspheres for the treatment and prevention of infections and osteomyelitis that may remain at the site of implantation and do not inhibit tissue regeneration.
Another object of this invention is to provide antibiotic microspheres for the treatment and prevention of infections that deliver antibiotics at the time of various surgical treatments to decrease the occurrence of infection
A further object of this invention is to provide antibiotic microspheres for the treatment and prevention of infections that can be easily and quickly implanted, injected, or otherwise placed totally or partially within the body at a site of actual or potential infection.
A still futher object of this invention is to provide antibiotic microspheres for the treatment and prevention of infections that can be placed at a site of at a site of placement of metal rods, plates or metallic fixators, of joint replacement devices, and of graft materials used in cardiovascular, general, gynecologic, and neurosurgical procedures.
Other objects of the invention will become apparent from time to time throughout the
specification and claims as hereinafter related.
The above noted objects and other objects of the invention are accomplished by the present biodegradable microspheres that are implanted, injected, or otherwise placed totally or partially within the body and are capable of near-linear controlled release of an antibiotic for a predetermined period of time for the treatment and prevention of infections involving the body. The microspheres are formed of polylactic-co-glycolic acid (PLGA) and an effective amount of antibiotic sufficient to produce bactericidal levels in body tissues, and may or may not include polyethylene glycol (PEG). The microspheres exhibit near-linear delivery of the antibiotic for at least 4 weeks at levels exceeding the minimum inhibitory concentration (MIC) for organisms commonly found to be the cause of infections. The microspheres allow antibiotics to be delivered at the time of various surgical treatments to decrease the occurrence of infection, and may be used for the treatment of open fractures, open reduction and internal fixation with metallic fixation of fractures, placement of joint replacement devices, and placement of various graft materials used in cardiovascular, general, gynecologic, and neurosurgical procedures.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a graph illustrating the in-vitro elution of the various microsphere formulations
Fig. 2 is a graph illustrating the results of a repeatability study of the in vitro elution rates where two of the formulations were manufactured more than one year apart.
Fig. 3 is a graph illustrating the in-vivo tobramycin concentrations in tissue over time foi" two of the formulations tested.
Fig. 4 is a graph illustrating the percentage of animals testing positive for osteomyelitis in a study of rabbits in groups treated with various antibiotic microsphere formulations.
Fig. 5 is a graph illustrating the results of radiographic and histological grading of the bone
specimens taken from the rabbit study.
Fig. 6 is a graph illustrating the concentration of tobramycin in the bones for the groups treated locally with tobramycin.
Fig. 7 is a graph illustrating the entrapment efficiency and elution rate over time of vaiious microsphere formulations utilizing vancomycin.
BEST MODE FOR CARRYING OUT THE INVENTION
rhe microsphere containing the antibiotic substance according to the present invention can be made of varying amounts of polylactic-co-glycolic acid (PLGA) with or without polyethylene glycol (PEG), and an effective cephalosporin antibiotic, using a water-in-oil-in-water (W/O/W), double-emulsion-solvent-extraction technique. In a preferred embodiment, the biodegradable microspheres are formed of from about 85% to about 99% by weight of polylactic-co-glycolic acid (PLGA) in a ratio of 50% lactic to 50% glycolic acid, from about 0% to about 5% by weight of polyethylene glycol (PEG); and an effective amount of an antibiotic agent sufficient to produce bactericidal levels in body tissues. The microspheres are characterized in that they exliibit near-linear delivery of the antibiotic agent for at least 4 weeks at levels exceeding the minimum inhibitory concentration (MIC) for organisms commonly found to be the cause of infections. The present invention will be more clearly understood with reference to the following examples, which are not to be construed to limit the scope of the invention.
EXAMPLE 1 - PLOA/tobramycin Drug Delivery System Preparation of Microspheres
In the following examples the polylactic-co-glycolic acid (PLGA) used was a high molecular weight blend of 50% lactic to 50% glycolic acid (Medisorb®), from Alkermes, Cincinnati, OH. Polyethylene glycol (PEG) and polyvinyl alcohol (PVA) were purchased from
Sigma Aldrich, of St. Louis, MO. Tobramycin (Nebcin®), from EH Lilly, Indianapolis, IN. was
purchased in powder form, and all remaining chemicals were purchased from Fisher Scientific
Microparticles were prepared in many blends of PLGA/PEQ/tobramycin using an established water-in-oil-in-water (W/O/W), double-emulsion-solvent-extraction technique. The size distribution of the microparticles was measured with a Coulter counter muitisizer (model 0646, Coulter Electronics, Hialeali, FL) after suspending the particles in an Isoton li solution (Coutler Electronics).
The entrapment efficiency of the formulation was determined in duplicate by normalizing the amount actually entrapped to the starting amount, using the established solvent-extraction technique. 1 Omg of microparticles was dissolved in 1ml of dichloromethane for 6 hours at room temperature. The tobramycin was then extracted from the organic phase to the aqueous phase by mixing 1ml PBS and removing the aqueous portion. This was repeated every six hours for twenty-four hours and all aqueous aliquots tested for tobramycin ooncentiation.
AH tobramycin concentrations were performed using fluorescence polarization immunoassay (Abbot TDx System). Sensitivity of the tobramycin assay is defined as the lowest measurable concentration which can be distinguished from zero with 95% confidence and was determined to be 0.18 microgram per milliliter. In-Vitro Elution Rate Determination
By dry weight, the percentage of PEG in the formulations was either 0% or .5%, and the percentage of tobramycin was either 1%, 5%, or 10%. In all, six different formulations were studied for tobramycin elution rates. 25mg amounts of microparticles were measured and placed into 2ml glass vials containing 1ml PBS, Each microparticle formulation was tested in triplicate and placed in a water bath at 37° C. After 24 hours, the vials were centrifuged and the
supernatant removed for tobramycin assay I ml of PBS was added to the vials and the vial
replaced in the water bath. This was repeated once daily for one week, and then every second
day for three additional weeks.
In-Vivo Drug Release Characteristics
Two formulations were studied in a mouse muscle pouch model, the 10% tobramycin with either 0% or 5% PEG. 60 adult female ICR mice, weigliing 20-24g were used for this investigation Each animal was anesthetized using ketamine (150mg/kg) and xylazine (6mg/kg) IP injection. A small incision was made over the right quadriceps muscle and a small pouch was made in the muscle by blunt dissection. In thirty mice, 5mg of microspheres containing 10% tobramycin and 0% PEG were implanted into the pouch; in the remaining thirty mice, microspheres containing 10% tobramycin and 5% PEG were implanted. Each pouch was closed with a nonabsorbable suture to mark the location. The skin was closed with resorbable suture All animals ambulated normally throughout the study, and no signs of local inflammation (swelling, tenderness) were visible.
For each of the two microsphere formulations tested, the mice were divided into 5 groups of six mice each and sacrificed sequentially at one day, four days, seven days, twenty-two days, and either 3.3 or 40 days post-surgery. At sacrifice, the scarred incision was reopened and the pouch located by the suture. Approximately 0.lg of tissue surrounding the suture was removed. Half of the tissue was placed in formalin for subsequent histological evaluation. The remaining half of the tissue was weighed and placed in 0.5ml PBS and macerated- The tissues from three mice in each group were randomly pooled together in each vial such that there were two vials for each timepoint for each group. The tissue was incubated for 2 hours at 37° C. After incubation, the vial was centrifuged and the supernatant filtered for tobramycin analysis. Tobramycin concentration is presented as amount of tobramycin per weight of muscJe tissue.
The preserved tissue was cut into 5|im sections and stained with an H&E stain. Each slide
was graded for inflammation by a blinded pathologist according to the following scale: 1 for no
01 minimal inflammation, 2 for moderate inflammation, and 3 for marked or severe
In Vitro Results
the in-vitro elation of the 6 microsphere formulations is shown in Fig 1. In this figure, the amount of drug released has been normalized to the total amount present in the implanted microspheres. The entrapment efficiency for each formulation of microsphere ranged between 40.24%) to 61.8%, as shown in Table 1 below. In general, adding PEG increased the entrapment efficiency. All microspheres were found to be on average 20 ± 1.6 µm in diameter.
Each formulation had a large initial release of tobramycin in the first 24 hours, followed by a few days of lowered release and then a few weeks of nearly steady release. Linear fits of the elution curves during the 7-28 day time period demonstrated correlations ranging from r^=0.7748 to 0.9770, indicating that the telease of antibiotic is very linear over this time period. Table 1 shows the calculated average linear release of tobramycin for each for-mulation for days 7 through 28 in absolute amounts and percentage of total amount of drug, Table 1. Microsphere Characteristics and in vitro Elution
We performed a repeatability study where two of the formulations were manufactured more
than one year apart. The in vitro elution rates for these experiments is presented in Fig 2.
In Vivo Results
The in-vivo tobramycin concentrations are shown in Fig. 3 for the two formulations tested.
The MIC of tobramycin against S. Aureus is shown for comparison. The histological scores for
the quadriceps tissue is shown in Table 2 below.
Table 2. Histological Scoring for Quadriceps Tissue (Table Removed)
The results of the in-vitro studies demonstrate that both changing the antibiotic concentration and the concentration of PEG can alter the elution characteristics of the antibiotic. In general, increasing the concentration of either component decreased the rate at which the antibiotic was released, although the initial burst of drug released increased with increasing antibiotic or PEG concentration. In all formulations the release rate leveled off to a near linear rate after the first week and remained steady for the next tluee weeks. At these linear release rates, it was determined that the formulation with 10% tobramycin and 0% PEG would have released all of the antibiotic in 60 days. By contrast, the formulation with 1% tobramycin and 0% PEG would take nearly 186 days to release all of the antibiotic. As can be seen from Fig 2, we can reproducibly manufacture the different microsphere formulations.
In results of the in-vivo study demonstrate that these microspheres do not elicit an extreme
information response The inflammation did increase to marked by day 3, but returned to
minimal levels by day 7 and remained there for the next three weeks. This inflammation was
localized to the implant site and did not produce visible signs of inflammation nor did it affect
the animal's appetite or ambulation.
The most important result was that although the in-vitro elution characteristics demonstrated a larger linear release rate of tobraniycin for the 10% tobramycin 5% PEG formulation, the in-vivo results showed higher tissue concentrations of tobramycin for the l0% tobramycin 0% PEG formulation, in fiact, although the tissue levels were measurable for the 10% tobramycin 5% PEG formulation tliroughout the study, they remained at or below the minimum inhibitory concentration (MIC) for aureus in the second through fourth week. By contrast, the 10% tobramycin 0% PEG formulation resulted in tissue concentrations at least twice the MIC for the entire study period.
Microspheres were visible with the histological examination indicating that the microspheres do remain at the site of implantation for at least thirty days, and indeed we found measurable tobramycin levels in the tissue for both formulations of microspheres throughout the length of the study.
The results of this study suggest that microspheres made of PLGA and tobramycin, with or without PEG, make a suitable biodegradable drug delivery system. These microspheres do not elicit an undesirable inflammatory response, and the formulation can be adjusted to vary the release kinetics of the antibiotic The microspheres deliver the antibiotic at a near-linear rate for at least four to six weeks. The microspheres remain at the site of implantation but are too small to inliibit tissue regeneration, a characteristic not shared by other suggested antibiotic delivery systems.
EXAMPLE 2 -PLGA/tobramvcin/PMMA - Parenteral Antibiotics
To test the effectiveness in eradicating an established case of osteomyelitis, a study was conducted using a rabbit model of osteomyelitis, wherein we tested the two methods of local antibiotic therapy - the microspheres and polymethyl methacrylate (PMMA) bone cement against parenteral antibiotics. Materials and Methods
Forty New Zealand White adult male rabbits, weighing 3-4 kg were selected for this study Each rabbit underwent an initial surgery to inoculate the radius with bacteria in a well-established procedure. Four weeks later, each rabbit was returned to the operating room for irrigatiou and debridement surgery and a wound culture. At the time of the second surgery, each animal was randomly placed into one of 5 groups for treatment of the infection: (1) Conlrol: control group treated with PLGA microspheres containing no antibiotic, (2). Microspheres: PLGA microspheres with 10% tobramycin,
(.3). Microspheres + Parenteral: PLGA microspheres with 10% tobramycin and parenteral Ancef,
(4). Cement + Parenteral: PMMA bead widi tobramycin and parenteral Ancef, and (5). Parenteral, parenteral Ancef.
Each animal underwent treatment for four weeks before sacrifice. AH animal procedures were approved by our institution's Animal Welfare Committee, Preparation of the PLGA Microspheres
The double emulsion solvent extraction teclmique, as described previously, was used to produce microspheres of approximately 15-20 µm in diameter containing approximately 10% by weight tobramycin (Nebcin®), from Eli Lilly, Indianapolis, IN. and 90% by weight 50:50 PLGA (Medisorb®), from Alkermes, Cincinnati, OH, These microspheres were blanketed with
nitrogen gas, placed in closed vials, and stored frozen at -70° C until used. Two days prior to
surgery the microspheres were sterilized using ethylene oxide gas. For each treated animal,
50mg of sterilized microspheres was implanted in the debrided bone defect.
Preparation of the PMMA Beads
At the time of irrigation and debridement surgery, PMMA beads were prepared by mixing 20g of polymethyl methacrylate bone cement (Orthoset®), from Wright Medical, Arlington, TN, with 0..6g of tobramycin (Nebcin®). The resulting mixture was formed into beads of approximately 4iTim diameter, weighing approximately OJg. One bead was placed into each debrided radius for treatment. Preparation of the .S. aureus Inoculate
The strain of S. aureus used in this study, UAMS-1, was isolated from a patient with osteomyelitis and deposited at the American Type Culture Collection as strain ATCC 49230. The bacteria were prepared from overnight cultures grown in tryptic soy broth at 37°C with aeration. Cells were harvested by centrifugation, washed with sterile physiological saline, and resuspended to a final concentration of 2 x l08 CFU/ml (OD of 60% transmittance). Cell suspensions were prepared on the day of surgery and held on ice until implanted.
Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) for the two antibiotics tested, tobramycin and cefazolin, were determined by standard dilution methods published by the National Committee for Clinical Laboratory Standards. Briefly, S aureus ceils were grown and diluted to 0.5 McFarland turbidity standard, approximately 2X10 cells/ml. The ceils were mixed with either of the two antibiotics tested, at concentrations ranging from 2ug/ml to 64ug/ml. The following day, the cultures were examined for turbidity to allow determination of MIC values. After this, sample clear cultures were plated to determine the MBC, and colonies counts were done the next day.
Surgical Procedure - Inoculation
All animals were fasted for 24 hours prior lo surgery. Anesthesia was induced with ketamine (40mg/lcg) and xylazine (0.5mg/kg) SQ injection. Anesthesia was maintained using isoflurane titrated to effect. The wound site was propped with betadine followed by a 70% ethanol rinse, and painted with Prepodyne prior to incision. The incision was made on anterior surface and extended down to the surface of the radius. The periosteum was sharply incised and elevated from the midshaft. A MicroHall oscillating saw was used to excise a 1 cm segment from the midshaft of the radius. An inoculum of 10µl(2xl06CPU) S aureus was delivered by microinjection with a sterile pipette tip with an outside diameter of 0.56mm directly into the center of the medullary canal. The segment was replaced in its original position and the wound closed. All animals were monitored daily for 4 weeks for food and water intake, ambulatory status, and presence of localized and systemic infection (wound swelling, fever, etc.), Surgical Procedure - Irrigation and Debridement
Four weeks following the date of the initial surgery, the animals were fasted and prepared for the second surgery. Surgical preparation was exactly the same. Once the wound was opened, the infected bone was swabbed and the swab sent for culture. All infected soft tissues and infected bone were removed. The wound was irrigated witlr 40cc normal saline through a syringe. If treatment involved a local drug delivery system (groups 1-4), this system was placed before the wound was closed.
Post-operative care included administration of 25 mg/kg cefazolin SC BID (Bums Veterinary Supply, Farmers Branch, TX) for animals in groups 3, 4, and 5 For groups 2, 3 and 4, serum and urine were collected tliree times/day for the first day, once a day for days 2-7, three times/week for week 2, twice/week for weeks 3 and 4. The collected serum and urine samples were assayed for tobramycin concentration. All tobramycin concentrations were performed
using fluorescence polarization immunoassay (Abbot TDx System), Sensitivity of the
tobramycin assay is defined as the lowest measurable concentration which can be distinguished
from zero with 95% confidence and was determined to be 0.18 microgram per milliliter.
Sacrifice and TestinH
All animals were sacrificed using an overdose of anesthesia (50-60mg/kg Pentobarbital
administered IV)., Weights were obtained If serum had not been obtained in the week
preceding sacrifice, it was obtained at the time of sacrificed and stored frozen until assayed. The
radius was removed from each animal and AP and lateral X-rays were obtained. Each x-ray was
labeled with tattoo number and the date. The radiographs were evaluated by two blinded
observers according to the radiographic grading scale shown in Table 3, belov/
Table 3. Radiographic Grading Scale
The forelimb was then stripped of skin and soft tissues and cultures were obtained by swabbing the defect site with a culturette, which was sent for species identification
Bone samples from the infected radius were divided so that both tobramycin assay and histology analysis could be performed. A 2cm piece of radius that surrounded the infection site was isolated using a Dremel saw. This section was divided into proximal and distal halves. One half was randomly chosen and pulverized after freezing in liquid nitrogen (MicroCryoCrusher®,
BioSpec Products, Bartlesville, OK). The pulverized bone was placed into a glass vial of known
weight, weighed and 0.5 cc of PBS was added. This sample was incubated in a 37°C water bath
for 2 hours. The sample was then filtered into a cryogenic container and refrigerated at 4°C until
the assay was performed. The remaining half was placed in a vial containing 10% NBF
Histological samples were decalcified, embedded in paraffin and sections were stained with
H&E and Gram stains. These slides were evaluated by a pathologist according to the grading
scale given in Table 4, below.
Table 4. Histological Grading Scale (Table Removed)
Tables 5 and 6 show the minimum inhibitory concentration (MIC) and minimum
bactericidal concentration (MBC) of tobramycin and cefazolin for this strain ofS aureus
bacteria The numbers are consistent with published values for strains of MRS A.
Table 6. MIC and MBC Determinations (Table Removed)
T= Tobramycin C= Cefazolin
All rabbits became infected after the inoculum surgery; 100% of the cultures taken at the irrigation and debridement surgery were positive for S aureus. Most animals developed signs of localized infection such as swelling or drainage at the surgical site but no animals showed signs of systemic disease. All animals were monitored daily for signs of discomfort and were treated to reduce discomfort. Supplemental food was given to animals with diminished appetite and rubber mats were placed in cages to make ambulation more comfortable. After treatment with parenteral cefazolin, some animals had to be treated with metronidazole (Flagyl®, Bums Veterinary Supply) for diarrhea. Tliree animals died prematurely due to diarrhea.
At sacrifice, the percentage of animals testing positive for osteomyelitis ranged from a maximum of 75% in the Control group (1) to a minimum of 25% in the Microspheres + Parenteral group (3) as shown in Fig. 4. Chi-square contingency table analysis shows that only the Microxpheres + Parenteral group (3) had a significantly lower percentage than the Control
group (1) (p= 046). However, if all of the groups where parenteral antibiotics were given are
lumped together, and the Control and Microspheres groups (1) and (2) are lumped together,
these are significantly different (p= 03.i).
Fig. 5 shows the results of the radiographic and histological grading of the specimens, in the radiographic grading scale, the Cement + Parenteral group (4) score significantly worse than the Control (1), Microspheres (2), and Parenteral (5) groups (p=.047) In the histological grading, none of the groups were significantly different.
Fig. 6 shows the concentration of tobramycin in the bones for the groups treated locally with tobramycin. At four weeks after implantation of the local carrier system, the microspheies were still releasing significant amounts of tobramycin The cement samples had small but measurable amounts of tobramycin. All but t'wo of the microsphere samples had concentrations of tobramycin above the MIC and near the MBC level for the bacteria tested, whereas none of the PMMA samples reached the MIC level. None of the tested serum and urine specimens had measurable levels of tobramycin.
We have developed and described herein, tobramycin-loaded microspheres as a biodegradable drug delivery system foi the treatment of osteomyelitis. These microspheres are spherical in shape with an average size of 20|im. The PLGA copolymers are biocompatible, biodegradable, and approved by the FDA for certain human clinical uses. !n~vitro and in-vivo testing in muscle demonstrated that these microspheres deliver antibiotics for longer than four weeks and at nearly linear rates.
We have demonstrated the effectiveness of tlrese microspheres in a rabbit model of osteomyelitis. In this study, all of the animals developed osteomyelitis by four weeks post inoculation- After the second surgery for irrigation and debridement of the wound, most of the animals showed signs of improvement, 25% of the animals in the Control group (1) showed no
signs of infection at sacrifice. The only treatment group to demonstrate a significant
impiovement over the Control was the Microspheres + Parenteral group (3), where 75%
percent of the animals showed no signs of infection at sacrifice. No treatment resulted in a
100% success rate.
Thus, the microspheres in accordance with the present invention resulted in high concentrations of tobramycin in the bone four weeks after implantation. The cement beads, by contrast, were still eluting tobramycin but at levels far below the MIC and MBC for the organism studied. In addition, the cement beads created a physical barrier against new bone formation in the debrided infection site. It was this phenomenon that resulted in the Cement + Parenteral group (4) having high (poorer) scores on the radiographic evaluation. Although the high bone tissue levels of tobramycin indicated that the microspheres remained at the site of implantation, the microspheres were small enough to allow new bone formation and degradation of the carrier (PLGA) occurred.
The histological scores indicated that there were no significant differences among any of the five groups studied. Thus, neither the microspheres nor the cement beads resulted in a clironic inflammatory response in the local tissues.
We have also demonstrated that these PLGA microspheres deliver antibiodc to the bone tissue at concentrations above or near the MBC for at least four weeks. At four weeks after the onset of treatment, the Microspheres + parenteral group (3) was the only group to demonstrate a significant improvement over the Control group (1), The microspheres in accordance with the present invention do not impede the formation of new bone growth into the debrided site, and do not require a second surgery for removal. The microspheres are biodegradable and do not result in clironic inflammation.
EXAMPLE 3 - PLGA/vancomycin/PMMA Microspheres
We performed studies similar to the examples and formulations described above, with vancomycin substituted for tobramycin. In these experiments, we produced microspheres of about 6,86µm (microns) in diameter containing approximately 5% by weight vancomycin, and microspheres of about 7.46µm (microns) in diameter containing approximately 10% by weight vancomycin, and 90% by weight 50:50 PLGA. The percentage of PEG in the Formulations was either 0% or 5%.
The results of the entrapment efficiencies and elution rates of vancomycin over a period of 600 hours ate presented in Fig. 7. The result was that over a 600 hour period, in the 10% vancomycin formulation approximately 27% of the vancomycin was eluted, and in the 5% vancomycin formulation approximately 40% of the vancomycin was eluted The entrapment efficiency of the 10% vancomycin formulation was found to be approximately 204% for the 10% vancomycin formulation and an entrapment efficiency of 21.5% for the 5% vancomycin formulation.
The vancomycin formulation, like the tobramycin formulation is eluted in a very good steady state manner. In both formulations, the levels were acceptable, with only slight differences in entrapment and release. Each of these formulations has advantages, for instance, one may be used as prophylaxis, while the other used for treatment of infection.
Although several antibiotics have been described herein for purposes of example, it should be understood the microspheres of die present invention may utilize various antibiotics and antibacterial agents or combinations thereof, preferably those in the class of "cephalosporins". These may be obtained commercially or be prepared according to the references cited in PHYSICIANS' DESK REFERENCE and the US FDA's Orange book.
For example, the present invention may utilize one or more of the following cornmercially
available antibiotics and antibacterial agents selected from the group consisting of; Ancef,
Tobramycin, Cefadioxil, Cefazolin, Cephalexin, Cefaclor, Cefotetan, Cefoxitin, Cefprozil,
Cefuioxime, Loracarbef, Cefdinir, Cefixinie, Cefopeiazone, Cefotaxime, Cefpodoxime,
Ceftazidime, Ceftibuten, Ceftozoxime, Ceftriaxone, Cefepime, and Vancomycin.
Tiie present controlled release antibiotic microspheres may be implanted injected, or otherwise placed totally oi partially within the body at a site of actual or potential infection and deliver an effective amount of the antibiotic agent sufficient to produce bactericidal levels in the body tissues and deliver a near-linear- dosage of the antibiotic for at least 4 weeks at levels exceeding the minimum inliibitoiy concentr-ation (MIC) for organisms commonly found to be the cause of the infections. The microspheres may be placed at a site of surgical treatment, such as a site of a bone fracture, at a site of placement of metal rods, plates or metallic fixators and joint replacement devices, or at a site of placement of graft materials used in cardiovascular, general, gynecologic, and neurosurgical procedures.
Wliile this invention has been described fully and completely with special emphasis upon preferred embodiments, it should be understood that within the scope of the appended claims the invention may be practiced otherwise than as specifically described herein,
1. Controlled release microspheres comprising:
biodegradable microspheres formed of from 85% to 99% by weight of polyiactic-co-glycolic acid (PLGA) in a ratio of 50% lactic to 50% glycolic acid and, optionally, from 0% to 5% by weight of polyethylene glycol (PEG); and an antibiotic agent entrapped in said microspheres and capable of being eluted from said microspheres wherein the microspheres are from about 6 µm to about 20 µm in diameter.
2. The controlled release microspheres as claimed in claim 1, wherein said antibiotic agent is 1% to 10% by weight of the microspheres.
3. The controlled release microspheres as claimed in claim 1, wherein said antibiotic agent is selected from the class of cephalosporin antibiotics.
4. The controlled release microspheres as claimed in claim 1, wherein said antibiotic agent is Ancef, Tobramycin, Cefadroxil, Cefazolin, Cephalexin, Cefactor, Cefotetan, Cefoxitin, Cefprozil, Cefuroxime, Loracarbef, Cefdinir, Cefixime, Cefoperazone, Cefotaxime, Cefpodoxime, Ceftazidime, Ceftibuten, Ceftozoxime, Ceftriaxone, Cefepime, or Vancomycin.
5. The controlled release microspheres as claimed in claim 1, wherein said microspheres are from about 15 µm to about 20 µm in diameter.
6. A method of making antibiotic microspheres, said method comprising:
entrapping an antibiotic, antibacterial agent, or combination thereof, in a polymer comprising 85-99 wt% PLGA and up to 5 wt% PEG to provide microparticles containing said antibiotic, antibacterial agent, or combination thereof; and
isolating said microparticles having a maximum diameter of 20 µm ±1.6 pm.
7. A drug delivery system comprising a multiplicity of microspheres comprising at least one antibiotic encapsulated in a polymeric membrane comprising polyethylene glycol (PEG) and polylactic-co-glycolic acid (PLGA), wherein said PLGA is a 50:50 blend of lactic acid and glycolic acid, said microspheres being capable of controlled release of said at least one antibiotic, antibacterial agent, or combination thereof.
|Indian Patent Application Number
|PG Journal Number
|Date of Filing
|Name of Patentee
|CATHERINE G. AMBROSE
|6431 FANNIN, HOUSTON, TEXAS 77030, U.S.A.
|PCT International Classification Number
|PCT International Application Number
|PCT International Filing date