Preparation and evaluation of cefuroxime axetil gastro-retentive floating drug delivery system via hot melt extrusion technology

被引:16
|
作者
Lalge, Rahul [1 ]
Thipsay, Priyanka [1 ]
Shankar, Vijay Kumar [1 ]
Maurya, Abhijeet [1 ]
Pimparade, Manjeet [1 ]
Bandari, Suresh [1 ]
Zhang, Feng [2 ]
Murthy, S. Narasimha [1 ,4 ]
Repka, Michael A. [1 ,3 ]
机构
[1] Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
[2] Univ Texas Austin, Coll Pharm, Austin, TX 78712 USA
[3] Univ Mississippi, Pii Ctr Pharmaceut Innovat & Instruct, University, MS 38677 USA
[4] Inst Drug Delivery & Biomed Res, Bangalore, Karnataka, India
基金
美国国家卫生研究院;
关键词
Cefuroxime axetil; Sustained release; Floating drug delivery systems; Pharmacokinetic study; Lipids; Enzymatic degradation; DOSAGE FORMS; SOLID DISPERSION; BIOAVAILABILITY; RESIDENCE; TRACT; PHARMACOLOGY; ABSORPTION; TABLETS; SITES; FOOD;
D O I
10.1016/j.ijpharm.2019.06.021
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cefuroxime Axetil (CA) is a poorly soluble, broad spectrum antibiotic which undergoes enzymatic degradation in gastrointestinal tract. The objective of the present study was to develop lipid-based gastro-retentive floating drug delivery systems containing CA using hot-melt extrusion (HME) to improve absorption. Selected formulations of CA and lipids were extruded using a twin screw hot-melt extruder. Milled extrudates were characterized for dissolution, floating strength, and micromeritic properties. Solid-state characterization was performed using differential scanning calorimetry (DSC), scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, and hot-stage microscopy. In vitro characterization demonstrated that the formulations exhibited a sustained drug release profile for 12 h. All formulations showed desired floating and flow properties. Solid-state characterization revealed no phase separation and no chemical interactions between the drug and excipients. Based on in vitro study results, an optimized formulation (F8) was further evaluated for in vivo performance. Oral bioavailability (C(ma)(x )and AUC(0)(-)(24h)) of F8 was significantly higher than that of pure CA. This study describes the use of lipid-based gastro-retentive floating drug delivery systems to achieve desired sustained release profile for more complete dissolution which could potentially reduce enzymatic degradation. This study also highlights the effectiveness of HME technology to improve dissolution and bioavailability.
引用
收藏
页码:520 / 531
页数:12
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