Stability of freeze-dried pH-responsive dextrin nanogels containing doxorubicin

被引:4
|
作者
Manchun, Somkamol [1 ,2 ]
Dass, Crispin R. [3 ,4 ]
Sriamornsak, Pornsak [1 ,2 ]
机构
[1] Silpakorn Univ, Dept Pharmaceut Technol, Fac Pharm, Nakhon Pathom 73000, Thailand
[2] Silpakorn Univ, Pharmaceut Biopolymer Grp PBiG, Fac Pharm, Nakhon Pathom 73000, Thailand
[3] Curtin Univ, Sch Pharm, Fac Hlth Sci, Perth, WA 6845, Australia
[4] Curtin Hlth Innovat Res Inst Ageing & Chron Dis, Bentley, WA 6102, Australia
关键词
Stability; Nanogels; Dextrin; DRUG-DELIVERY; NANOPARTICLES; DEGRADATION; HYDROGELS; CANCER; DESIGN;
D O I
10.1016/j.ajps.2015.09.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Induction of non-specific toxicities by doxorubicin (DOX) has restricted conventional DOX-based chemotherapy. pH-responsive dextrin nanogels (DNGs) have been fabricated in order to incorporate and deliver DOX to specific (targeted) sites. However, adequate stability studies of DOX-loaded DNGs are required for selection of storage conditions. The aim of this study was therefore to evaluate the accelerated (25 degrees C/60% RH) and long-term (5 degrees C) stability of DNGs prepared with formaldehyde (FDNGs) and glyoxal (GDNGs) as cross-linker by determining the change in their physicochemical properties. The mean diameter decreased with time during long-term storage. The drug content between freshly prepared (initial day) and after storage at 5 degrees C for 180 days of DOX-loaded FDNGs and DOX-loaded GDNGs was not significantly different (p > 0.05), but decreased after storage under the accelerated condition. The release of DOX from all DNGs was pH-dependent. However, DNGs kept under the accelerated condition showed higher amount of DOX release than those stored at 5 degrees C and the freshly prepared ones. The results indicate that the stability of DNGs could be improved by their storage at 5 degrees C. (C) 2016 The Authors. Production and hosting by Elsevier B.V. on behalf of Shenyang Pharmaceutical University.
引用
收藏
页码:648 / 654
页数:7
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