Cross-linked guar gum and sodium borate based microspheres as colon-targeted anticancer drug delivery systems for 5-fluorouracil

被引:0
作者
Kamal, Tehsin [1 ]
Sarfraz, Muhammad [2 ]
Arafat, Mosab [2 ]
Mikov, Momir [3 ]
Nisar-ur-Rahman [1 ]
机构
[1] COMSATS Inst Informat Technol, Dept Pharm, Abbottabad, Pakistan
[2] Al Ain Univ Sci & Technol, Coll Pharm, Abu Dhabi, U Arab Emirates
[3] Univ Novi Sad, Dept Pharmacol Toxicol & Clin Pharmacol, Med Fac, Novi Sad, Serbia
关键词
5-Fluorouracil; micro spheres; guar gum; colon drug delivery; anticancer delivery; sodium borate; IN-VIVO EVALUATION; DIHYDROPYRIMIDINE DEHYDROGENASE; 5-ETHYNYLURACIL; 776C85; VITRO; RELEASE; DESIGN; PHARMACOKINETICS; HYDROGEL; RHEOLOGY; COMPLEX;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim was to prepare cross linked polymer of 5-fluorouracil loaded microspheres containing guar gum and sodium borate for colon-targeted drug delivery systems. Micro spheres were prepared using emulsification cross linking method. The influence of drug polymer ratio, cross linker agent concentrations and cross linking timing on in vitro drug release and characteristics in terms of drug loading, entrapment efficiency and yielding percentage were investigated. The optimum drug loading, entrapment efficiency and percent yield were obtained from formulations with the lowest content of cross linker agent over 2 h of cross linking timing but with the highest drug to polymer ratio 1:11. The optimum in vitro drug release was obvious upon decreasing drug to polymer ratio up to 1:09, resulting in 81.5% drug release over 24 h. In conclusion, micro spheres composed of gaur gum and sodium borate can delay and control the release of 5-fluorouracil over 24 h. Thus, further in vivo studies are suggested for final assessment.
引用
收藏
页码:2329 / 2336
页数:8
相关论文
共 42 条
[1]  
[Anonymous], GOODMAN GILMANS
[2]  
[Anonymous], 2016, GLOB DRUGS THERAP
[3]  
Arafat M, 2012, BILOSOMES DRUG DELIV
[4]  
Arafat M., 2015, Int J Pharm Pharm Sci, V7, P16
[5]   Nanosized Liposomes Containing Bile Salt: A Vesicular Nanocarrier for Enhancing Oral Bioavailability of BCS Class III Drug [J].
Arafat, Mosab ;
Kirchhoefer, Cathrin ;
Mikov, Momir ;
Sarfraz-, Muhammad ;
Lobenberg, Raimar .
JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES, 2017, 20 :305-318
[6]   Mixed Micelles Loaded with Bile Salt: An Approach to Enhance Intestinal Transport of the BCS Class III Drug Cefotaxime in Rats [J].
Arafat, Mosab ;
Kirchhoefer, Cathrin ;
Mikov, Momir .
EUROPEAN JOURNAL OF DRUG METABOLISM AND PHARMACOKINETICS, 2017, 42 (04) :635-645
[7]  
Bhat Subramanya K., 2013, PHARM CHEM, V5, P221
[8]  
CAO SS, 1994, CANCER RES, V54, P1507
[9]  
Chandra SE, 2011, J APPL PHARM SCI, V1, P199
[10]   Design and development of multiparticulate system for targeted drug delivery to colon [J].
Chourasia, MK ;
Jain, SK .
DRUG DELIVERY, 2004, 11 (03) :201-207