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

Background: Microspheres of gelatin-A and κ-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.

[1]  K. Sawant,et al.  Development, optimization and in vitro evaluation of alginate mucoadhesive microspheres of carvedilol for nasal delivery , 2009, Journal of microencapsulation.

[2]  T. Maji,et al.  Preparation of genipin cross-linked chitosan-gelatin microcapsules for encapsulation of Zanthoxylum limonella oil (ZLO) using salting-out method , 2008, Journal of microencapsulation.

[3]  H. Park,et al.  Characterizations of fish gelatin films added with gellan and κ-carrageenan , 2007 .

[4]  K. Prasad,et al.  Effect of genipin, a naturally occurring crosslinker on the properties of kappa-carrageenan. , 2007, International journal of biological macromolecules.

[5]  T. Maji,et al.  Microencapsulation of Zanthoxylum limonella oil (ZLO) in glutaraldehyde crosslinked gelatin for mosquito repellent application. , 2007, Bioresource technology.

[6]  D. Barends,et al.  Biowaiver monographs for immediate release solid oral dosage forms: isoniazid. , 2007, Journal of pharmaceutical sciences.

[7]  A. Périchaud,et al.  Segmented polyurethane-based microparticles: Synthesis, properties, and isoniazid encapsulation and kinetics of release , 2006 .

[8]  Keishiro Tomoda,et al.  Effects of pulmonary surfactant system on rifampicin release from rifampicin-loaded PLGA microspheres. , 2005, Colloids and surfaces. B, Biointerfaces.

[9]  Kwaku G. Duodu,et al.  Fourier transform infrared (FTIR) spectroscopic study of acid soluble collagen and gelatin from skins and bones of young and adult Nile perch (Lates niloticus) , 2004 .

[10]  R. Pandey,et al.  Subcutaneous nanoparticle-based antitubercular chemotherapy in an experimental model. , 2004, The Journal of antimicrobial chemotherapy.

[11]  K. Yao,et al.  A novel pH‐sensitive gelatin–DNA semi‐interpenetrating polymer network hydrogel , 2004 .

[12]  T. Aminabhavi,et al.  Controlled release of clozapine through chitosan microparticles prepared by a novel method. , 2004, Journal of controlled release : official journal of the Controlled Release Society.

[13]  R. Pandey,et al.  Chemotherapeutic potential of alginate-chitosan microspheres as anti-tubercular drug carriers. , 2004, The Journal of antimicrobial chemotherapy.

[14]  Hsing-Wen Sung,et al.  Crosslinking structures of gelatin hydrogels crosslinked with genipin or a water‐soluble carbodiimide , 2004 .

[15]  Li Zhuo,et al.  FACTORS AFFECTING THE PARTICLE SIZE AND SIZE DISTRIBUTION OF POLYUREA MICROCAPSULES BY INTERFACIAL POLYMERIZATION OF POLYISOCYANATES , 2004 .

[16]  Ninad S. Save,et al.  Stimuli sensitive copolymer poly(N-tert-butylacrylamide-ran-acrylamide): processing into thin films and their transitional behaviour , 2003 .

[17]  Rajesh Pandey,et al.  Poly (DL-lactide-co-glycolide) nanoparticle-based inhalable sustained drug delivery system for experimental tuberculosis. , 2003, The Journal of antimicrobial chemotherapy.

[18]  Sadhna Sharma,et al.  Chemotherapeutic Potential of Orally Administered Poly(Lactide-Co-Glycolide) Microparticles Containing Isoniazid, Rifampin, and Pyrazinamide against Experimental Tuberculosis , 2003, Antimicrobial Agents and Chemotherapy.

[19]  C. Lii,et al.  Electrosynthesis of κ-Carrageenan Complexes with Gelatin , 2003 .

[20]  Mansoor Amiji,et al.  Chitosan-based gastrointestinal delivery systems. , 2003, Journal of controlled release : official journal of the Controlled Release Society.

[21]  Yen Chang,et al.  A genipin-crosslinked gelatin membrane as wound-dressing material: in vitro and in vivo studies , 2003, Journal of biomaterials science. Polymer edition.

[22]  R. C. Evangelista,et al.  Microspheres of alginate-chitosan containing isoniazid. , 2003, Journal of microencapsulation.

[23]  S. Garg,et al.  Role of poly [DL-lactide-co-glycolide] in development of a sustained oral delivery system for antitubercular drug(s). , 2002, International journal of pharmaceutics.

[24]  K. Zhu,et al.  Controlled drug release properties of ionically cross-linked chitosan beads: the influence of anion structure. , 2002, International journal of pharmaceutics.

[25]  A. R. Kulkarni,et al.  Crosslinked chitosan microspheres for encapsulation of diclofenac sodium: effect of crosslinking agent , 2002, Journal of microencapsulation.

[26]  G. Khuller,et al.  Liposomes and PLG microparticles as sustained release antitubercular drug carriers--an in vitro-in vivo study. , 2001, International journal of antimicrobial agents.

[27]  A. Fauci,et al.  Infectious diseases: considerations for the 21st century. , 2001, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[28]  R. Fitzpatrick,et al.  Determination of amino acids in diverse polymeric matrices using HPLC, with emphasis on agars and agaroses. , 1999, Biochimica et biophysica acta.

[29]  C. Nastruzzi,et al.  Liposomes, micelles and microemulsions as new delivery systems for cytotoxic alkaloids. , 1999, Pharmaceutical science & technology today.

[30]  G. Goissis,et al.  Biocompatibility studies of anionic collagen membranes with different degree of glutaraldehyde cross-linking. , 1999, Biomaterials.

[31]  H. Sung,et al.  In vitro evaluation of cytotoxicity of a naturally occurring cross-linking reagent for biological tissue fixation. , 1999, Journal of biomaterials science. Polymer edition.

[32]  G. Banerjee,et al.  A Novel Peptide-Grafted Liposomal Delivery System Targeted to Macrophages , 1998, Antimicrobial Agents and Chemotherapy.

[33]  A. Florence,et al.  The preparation and properties of niosomes—non‐ionic surfactant vesicles , 1985, The Journal of pharmacy and pharmacology.

[34]  H. Reiss Entropy-induced dispersion of bulk liquids , 1975 .