Microencapsulation of isoniazid in genipin-crosslinked gelatin-A-κ-carrageenan polyelectrolyte complex

被引:34
作者
Devi, Nirmala [1 ]
Maji, Tarun K. [1 ]
机构
[1] Tezpur Univ, Dept Chem Sci, Napaam 784028, Assam, India
关键词
Controlled release; genipin; isoniazid; microspheres; polyelectrolyte complex; LACTIDE-CO-GLYCOLIDE; LIMONELLA-OIL ZLO; DELIVERY-SYSTEM; CHITOSAN MICROSPHERES; ALGINATE-CHITOSAN; IN-VITRO; RELEASE; MICROPARTICLES; ENCAPSULATION; LIPOSOMES;
D O I
10.3109/03639040903061355
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Microspheres of gelatin-A and kappa-carrageenan were prepared by using genipin, a naturally occurring crosslinker, and sunflower oil as reaction media. Method: The variations in the size of the microspheres formed by varying the amount of surfactant (0.33-1.0 g/g of polymer), polymer (1.5-3.0 g), and crosslinker (0.2-0.8 mmol) were studied by scanning electron microscopy. The encapsulation of isoniazid was carried out by absorption. The isoniazid content in the prepared microspheres was determined. The release characteristic of isoniazid was also studied at pH values 1.2 and 7.4 by using UV-spectrophotometer. Results: Characterization of the isoniazid-loaded microspheres was carried out by using Fourier transform infrared spectrophotometry, differential scanning calorimetry, and X-ray diffractometery.
引用
收藏
页码:56 / 63
页数:8
相关论文
共 35 条
[1]   Controlled release of clozapine through chitosan microparticles prepared by a novel method [J].
Agnihotri, SA ;
Aminabhavi, TM .
JOURNAL OF CONTROLLED RELEASE, 2004, 96 (02) :245-259
[2]  
Ain Q, 2002, INT J PHARM, V239, P37, DOI 10.1016/S0378-5173(02)00034-0
[3]   THE PREPARATION AND PROPERTIES OF NIOSOMES NON-IONIC SURFACTANT VESICLES [J].
BAILLIE, AJ ;
FLORENCE, AT ;
HUME, LR ;
MUIRHEAD, GT ;
ROGERSON, A .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1985, 37 (12) :863-868
[4]  
Banerjee G, 1998, ANTIMICROB AGENTS CH, V42, P348
[5]   Biowaiver monographs for immediate release solid oral dosage forms: Isoniazid [J].
Becker, C. ;
Dressman, J. B. ;
Amidon, G. L. ;
Junginger, H. E. ;
Kopp, S. ;
Midha, K. K. ;
Shah, V. P. ;
Stavchansky, S. ;
Barends, D. M. .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 96 (03) :522-531
[6]   A genipin-crosslinked gelatin membrane as wound-dressing material:: in vitro and in vivo studies [J].
Chang, WH ;
Chang, Y ;
Lai, PH ;
Sung, HW .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2003, 14 (05) :481-495
[7]   Liposomes, micelles and microemulsions as new delivery systems for cytotoxic alkaloids [J].
Cortesi, R ;
Nastruzzi, C .
PHARMACEUTICAL SCIENCE & TECHNOLOGY TODAY, 1999, 2 (07) :288-298
[8]   Liposomes and PLG microparticles as sustained release antitubercular drug carriers - an in vitro-in vivo study [J].
Dutt, M ;
Khuller, GK .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2001, 18 (03) :245-252
[9]   Infectious diseases: Considerations for the 21st century [J].
Fauci, AS .
CLINICAL INFECTIOUS DISEASES, 2001, 32 (05) :675-685
[10]   Biocompatibility studies of anionic collagen membranes with different degree of glutaraldehyde cross-linking [J].
Goissis, G ;
Junior, EM ;
Marcantônio, JAC ;
Lia, RCC ;
Cancian, DCJ ;
de Carvalho, M .
BIOMATERIALS, 1999, 20 (01) :27-34