RRC ID 65730
著者 Peng J, Fumoto S, Miyamoto H, Chen Y, Kuroda N, Nishida K.
タイトル One-step formation of lipid-polyacrylic acid-calcium carbonate nanoparticles for co-delivery of doxorubicin and curcumin.
ジャーナル J Drug Target
Abstract A doxorubicin (Dox) and curcumin (Cur) combination treatment regimen has been widely studied in pre-clinical research. However, the nanoparticles developed for this combination therapy require a consecutive drug loading process because of the different water-solubility of these drugs. This study provides a strategy for the "one-step" formation of nanoparticles encapsulating both Dox and Cur. We took advantage of polyacrylic acid (PAA) and calcium carbonate (CaCO3) to realise a high drug entrapment efficiency (EE) and pH-sensitive drug release using a simplified preparation method. Optimisation of lipid ratios and concentrations of CaCO3 was conducted. Under optimal conditions, the mean diameter of PEGylated lipid/PAA/CaCO3 nanoparticles with encapsulated Cur and Dox (LPCCD) was less than 100 nm. An obvious pH-sensitive release of both drugs was observed, with different Dox and Cur release rates. Successful co-delivery of Cur and Dox was achieved via LPCCD on HepG2 cells. LPCCD altered the bio-distribution of Dox and Cur in vivo and decreased Dox-induced cardiotoxicity. The current investigation has developed an efficient ternary system for co-delivery of Dox and Cur to tumours, using a "one-step" formation resulting in nanoparticles possessing remarkable pH-sensitive drug release behaviour, which may be valuable for further clinical studies and eventual clinical application.
巻・号 25(8)
ページ 704-714
公開日 2017-9-1
DOI 10.1080/1061186X.2017.1315687
PMID 28368667
MeSH Acrylic Resins / chemistry* Animals Calcium Carbonate / chemistry* Curcumin / administration & dosage* Doxorubicin / administration & dosage* Hep G2 Cells Humans Lipids / chemistry* Male Mice Nanoparticles / chemistry* Rats Rats, Wistar
IF 3.38
リソース情報
ヒト・動物細胞 Hep G2(RCB1886)