Synthetic, implantable, biodegradable polymers for controlled release of radiosensitizers

被引:13
作者
Yuan, X
Fahlman, C
Tabassi, K
Williams, JA
机构
[1] Johns Hopkins Univ, Sch Med, Johns Hopkins Oncol Ctr, Dept Oncol,Div Radiat Oncol,Radiobiol Lab, Baltimore, MD 21205 USA
[2] Johns Hopkins Hosp, Dept Neurosurg, Brain Tumor Res Lab, Baltimore, MD 21287 USA
关键词
polymer; radiosensitizer; radiotherapy; controlled release; malignant brain neoplasms;
D O I
10.1089/cbr.1999.14.177
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Synthetic implantable, biodegradable polymers offer the sustained focal release of disparate therapeutic agents for the treatment of human malignant brain rumors. The role of polymeric devices for the local delivery of radiosensitizers remains unexplored however We therefore quantified the release of the representative radiosensitizers IUdR (5-iodo-2'-deoxyuridine), tirapazamine (3-amino-1,2,4-benzotriazine-1, 4-dioxide) and etanidazole [N-(2-hydroxyethyl)-2-nitro-1-imidazole-1-acetamide] from the [(poly(bis(p-carboxyphenoxyl-propane) (PCPP):sebacic acid (SA) (PCPP:SA ratio 20:80)] polymer. Methods: For measurements of controlled release, triplicate polymer discs were incubated for known intervals in 2 mi 0.1 phosphate-buffered saline, pH 7.4, 37 degrees C. Using a predefined schedule, the supernatant fractions were systematically removed and replaced with fresh solution. The supernatant fractions were measured The cumulative percentage of the loaded drug that appeared in these serial supernatant fractions was plotted vs. time. The percentage of the drug that was loaded into each polymer and that was released vs. time was fit to the power function of the form y = (a) *t(b), where y is the cumulative released agent, a and b are constants and t is time (days). Results: The IUdR was released over an interval of approximately one week, while the release of the tirapazimine persisted for over 100 days. The etanidazole was released most rapidly, over a period of hours. Modeling of release showed that regardless of percentage loading of the drug the monoexponential function showed high correlation of the fit of the plot of the release vs, time. Conclusions: These results suggest that the hydrophilicity and percentage loading of the drug predominantly determine the rate of release. Based upon these results, IUdR and tirapazamine warrant preclinical testing for radiosensitization of human malignant brain rumors via the synthetic implantabte, biodegradable polymeric devices.
引用
收藏
页码:177 / 186
页数:10
相关论文
共 57 条
[1]  
Akbari H, 1998, Pharm Dev Technol, V3, P251, DOI 10.3109/10837459809028502
[2]   REGROWTH PATTERNS OF GLIOBLASTOMA-MULTIFORME RELATED TO PLANNING OF INTERSTITIAL BRACHYTHERAPY RADIATION-FIELDS [J].
BASHIR, R ;
HOCHBERG, F ;
OOT, R .
NEUROSURGERY, 1988, 23 (01) :27-30
[3]   BIOCOMPATIBILITY OF A BIODEGRADABLE, CONTROLLED-RELEASE POLYMER IN THE RABBIT BRAIN [J].
BREM, H ;
KADER, A ;
EPSTEIN, JI ;
TAMARGO, RJ ;
DOMB, A ;
LANGER, R ;
LEONG, KW .
SELECTIVE CANCER THERAPEUTICS, 1989, 5 (02) :55-65
[4]   PLACEBO-CONTROLLED TRIAL OF SAFETY AND EFFICACY OF INTRAOPERATIVE CONTROLLED DELIVERY BY BIODEGRADABLE POLYMERS OF CHEMOTHERAPY FOR RECURRENT GLIOMAS [J].
BREM, H ;
PIANTADOSI, S ;
BURGER, PC ;
WALKER, M ;
SELKER, R ;
VICK, NA ;
BLACK, K ;
SISTI, M ;
BREM, S ;
MOHR, G ;
MULLER, P ;
MORAWETZ, R ;
SCHOLD, SC .
LANCET, 1995, 345 (8956) :1008-1012
[5]   SR-4233 (TIRAPAZAMINE) - A NEW ANTICANCER DRUG EXPLOITING HYPOXIA IN SOLID TUMORS [J].
BROWN, JM .
BRITISH JOURNAL OF CANCER, 1993, 67 (06) :1163-1170
[6]  
BROWN JM, 1990, CANCER RES, V50, P7745
[7]  
Brown JM, 1998, CANCER RES, V58, P1408
[8]  
CHANG CH, 1983, CANCER, V52, P997, DOI 10.1002/1097-0142(19830915)52:6<997::AID-CNCR2820520612>3.0.CO
[9]  
2-2
[10]   MATHEMATICAL-MODELS FOR RELEASE OF DRUGS FROM MATRIX TABLETS [J].
COBBY, J .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1978, 12 (05) :627-634