BIODEGRADABLE CONTROLLED ANTIBIOTIC RELEASE DEVICES FOR OSTEOMYELITIS - OPTIMIZATION OF RELEASE PROPERTIES

被引:143
作者
ZHANG, XC
WYSS, UP
PICHORA, D
GOOSEN, MFA
机构
[1] QUEENS UNIV,DEPT CHEM ENGN,KINGSTON K7L 3N6,ON,CANADA
[2] QUEENS UNIV,DEPT MECH ENGN,KINGSTON K7L 3N6,ON,CANADA
[3] QUEENS UNIV,DEPT SURG,KINGSTON K7L 3N6,ON,CANADA
关键词
D O I
10.1111/j.2042-7158.1994.tb03890.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Controlled antibiotic release films, melt-extruded cylinders, and suspension-extruded/coated cylinders were manufactured from biodegradable poly(D,L-lactide) (PDLLA) and poly(D,L-lactide-CO-epsilon-caprolactone). These devices have potential application in the treatment of osteomyelitis. The in-vitro release properties of the devices were examined with drug loadings varying from 16 to 50%. Gentamicin sulphate films and melt-extruded gentamicin/PDLLA cylinders demonstrated a large initial burst and incomplete release. The films and melt-extruded cylinders made from poly(D,L-lactide-CO-epsilon-caprolactone), low mol. wt poly(D,L-lactide), and a mixture of D,L-lactic acid oligomer and high mol. wt poly(D,L-lactide), did not remain intact during the entire release period. While this is undesirable, these materials do have the advantage of not requiring a processing temperature of greater than 110 degrees C. Antibiotic release from high mol. wt PDLLA-coated gentamicin/PDLLA cylinders, with 40 and 50% loading, was very rapid. The antibiotic could only diffuse out through the open ends of the cylinder. Coated gentamicin sulphate cylinders with 20 and 30% drug loading gave the most promising properties in terms of a small initial burst, and a gradual and sustained release. The release rate and duration from the coated cylinders could be adjusted by cutting the cylinder into different lengths; the time required for 90% of the entrapped gentamicin to be released into water from 30% loaded PDLLA-coated cylinders 0.2, 0.4, 0.7 and 1 cm in length was 1000, 1700, 2300, and 2800 h, respectively. This offers a convenient method to adjust the release to meet the specific antibiotic requirement of different patients. Cephazolin and benzylpenicillin were found to be unsuitable for sustained release longer than 300 h due to the hydrolytic instability of the drugs in water.
引用
收藏
页码:718 / 724
页数:7
相关论文
共 24 条
[1]  
BAILEY JE, 1986, BIOCH ENG FUNDAMENTA, P384
[2]   N-FORMYLPENICILLAMINE AND PENICILLAMINE AS DEGRADATION PRODUCTS OF PENICILLINS IN SOLUTION [J].
BIRD, AE ;
JENNINGS, KR ;
MARSHALL, AC .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1986, 38 (12) :913-916
[3]   NEW SPECTROPHOTOMETRIC METHOD FOR DETERMINATION OF PENICILLINS [J].
BUNDGAARD, H ;
ILVER, K .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1972, 24 (10) :790-+
[4]  
COOMBS R, 1989, INFECTION ORTHOPAEDI
[5]   BIODEGRADABLE IMPLANTS CONTAINING GENTAMICIN - DRUG RELEASE AND PHARMACOKINETICS [J].
FIRSOV, AA ;
NAZAROV, AD ;
FOMINA, IP .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1987, 13 (9-11) :1651-1674
[6]  
IKADA Y, 1985, Journal of Controlled Release, V2, P179, DOI 10.1016/0168-3659(85)90043-4
[7]   AMINO-ACID-ANALYSIS AND ENZYMATIC SEQUENCE DETERMINATION OF PEPTIDES BY AN IMPROVED ORTHO-PHTHALDIALDEHYDE PRE-COLUMN LABELING PROCEDURE [J].
JONES, BN ;
PAABO, S ;
STEIN, S .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1981, 4 (04) :565-586
[8]   STRUCTURE PROPERTY RELATIONSHIPS IN THE CASE OF THE DEGRADATION OF MASSIVE ALIPHATIC POLY-(ALPHA-HYDROXY ACIDS) IN AQUEOUS-MEDIA .1. POLY(DL-LACTIC ACID) [J].
LI, SM ;
GARREAU, H ;
VERT, M .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 1990, 1 (03) :123-130
[9]   HYDROXYLAMINE DETERMINATION OF CEPHALOSPORINS [J].
MAYS, DL ;
BANGERT, FK ;
CANTRELL, WC ;
EVANS, WG .
ANALYTICAL CHEMISTRY, 1975, 47 (13) :2229-2234
[10]  
PITT CG, 1981, BIOMATERIALS, V2, P215