Preparation of lung targeting microspheres of gelatin ceftiofur alkali

被引:0
作者
Zhihui Hao
Yongda Zhao
Baohan Qu
Haoting Wu
Lihua Hao
Zhaopeng Ding
Fenfang Yang
机构
[1] Qingdao Agricultural University,Laboratory of Chemical and Biological, College of Chemistry and Pharmacy
[2] Qingdao Continent Pharmaceutical Co. Ltd.,undefined
[3] China Institute of Veterinary Drug Control,undefined
来源
Journal of Wuhan University of Technology-Mater. Sci. Ed. | 2013年 / 28卷
关键词
gelatin ceftiofur alkali microsphere; lung targeting; microsphere morphology;
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中图分类号
学科分类号
摘要
Gelatin ceftiofur alkali microsphere was prepared to observe its characteristics and evaluate preservation conditions. The glutaraldehyde was increased and the carboxylic methyl chitosan was added to improve the microsphere. The experimental results show microspheres have a better morphology surface and fairly regular structure with 4% glutaraldehyde. The average particle size is 15.84 μm and particle size distribution is narrow which shows a good uniformity. Microsphere size was affected by the stirrer speed, dosing ratio and curing degree. The greater drug loaded is, the better microspheres loading is; but with the increase of drug loading rate, the entrapment efficiency increases first and then decreases. The drug release rate of the microsphere is 24.90% in 0.5 h and 84.90% in 48 h, when CMC-GMs with 4% curing agent is 32.03% in 0.5 h and 88.44% in 48 h. So Gms embedding of ceftiofur alkali are better than CMC-GM. The stability tests show that strong light, high temperature, high humidity have a great influence on the microspheres.
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页码:400 / 405
页数:5
相关论文
共 29 条
[1]  
Lepeniotis S(1997)Synthesis of Starch Acetate: Statistical Designed Experiments to Optimize the Reaction Conditions[J] Chemometrics and Intelligent Laboratory Systems 36 229-243
[2]  
Feuer B I(1999)Optimization of the Encapsulation and Release of International Journal of Pharmaceutics 183 67-71
[3]  
Rojas J(1978)-lactoglobulin Entrapped Poly(dl· Iactide-co-glycolide)Microspheres[J] Proc. Natl. Acad. Sci. USA 75 4 194-4 198
[4]  
Pinto-Alphandary H(1992)Procedure for Preparation of Liposomes with Large Internal Aqueous Space and High Capture by Reverse-phaseevaporation[ J] Card. Vet. Res. 56 267-274
[5]  
Leo E e a1(1976)PhamacoldnetiCS of Ceftiofur in Serum, Tissue, Chamber Fluid and Bronchial Secretions form Healthy Beef-bred Catles[J] Biochim. Biophys. Acta 457 259-302
[6]  
Szoka FJR(1989)New Aspects Ofliposomes[J] Biochemistry 28 4 240-4 244
[7]  
Vapahadjopoulos D(1998)Quantitative Fluorescence Measurement of Chloride Transport Mechanisms in Phospholipid Vesicles[J] J. Dairy Sci. 81 15, 55-62
[8]  
Halstead SL(2007)Comparison of Various Antibiotic Treatment for COWS Diagnosed with Toxic Puetpetal Metritis[J] Internal Journal of Pharmaeeutics 337 118-126
[9]  
Walker RD(2006)Efect of Mearl Diameter and Polydispersity of PLGA Microspheres on Dmg Release: Experiment and Theory[J] Journal of Controlled Release 112 293-300
[10]  
Baker J e a1(2011)Elevated Temperature Accelerated Release Testing of PI. GA Mierospheres[J] Antimicrob Agents Chemother 55 4 990-4 998