Enhanced oral bioavailability through nanotechnology in Saudi Arabia: A meta-analysis

被引:6
作者
Al Jbour, Nawzat D. [1 ]
机构
[1] Middle East Univ, Fac Pharm, Amman, Jordan
关键词
Nanoformulation; Nanoparticle; Nanotechnology; Oral bioavailability; Pharmacokinetic parameters; Saudi Arabia; DRUG-DELIVERY SYSTEMS; SOLID LIPID NANOPARTICLES; CYCLOSPORINE-A; SILDENAFIL CITRATE; SUSTAINED-RELEASE; IN-VIVO; LIPOSOMES; MICELLES; HETEROGENEITY; NANOCARRIERS;
D O I
10.1016/j.arabjc.2022.103715
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Oral administration represents the most suitable mean among different means of administering drugs because it ensures high compliance by patients. Nevertheless, the lacking aqueoussolubility, as well as, inadequate metabolic/enzymatic stability of medicines are leading obstacles to successful drug administration by oral route. Among different systems, drug administration systems based on nanotechnology have the potential to surmount the problems associated with oral drug administration. Drug delivery systems based on nanotechnology offer an alternative to deliver antihypertensive agents with enhanced therapeutic effect and bioavailability. In this study, meta analysis was utilized in combining data relating to oral bioavailability (area under plasma concentration time curve, AUC) enhancement through nanotechnology from multiple studies. Twenty-one studies of the total 37articles included in this study were from the kingdom of Saudi Arabia and were included in a specific meta-analysis. From the analysis conducted, the overall enhancement power of the nanotechnology based formulations on drug bioavailability was found to be 7.94% (95 %CI [5.809, 10.064]). Haven utilized comprehensive and recent data of the confirmed the enhancement of bioavailability using nanotechnology which for this study was grouped into five: solid lipid nanoparticles; polymer based nanoparticles; SNEEDS/Nanoemulsion; liposomes/proliposomes and; nanostructured lipid carriers. Furthermore, the meta-analysis, provided evidence of insignificant differences between APG Bio-SNEDDS and its free drug suspension (Apeginin, APG), though with relative bioavailabiilty of 1.91. Notwithstanding most of the treatment showed a substantial relative bioavailability.(c) 2022 The Author. Published by Elsevier B.V. on behalf of King Saud University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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页数:13
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