However, limited work of A2B2 and A3B3 type miktoarm polymers was reported on drug and gene delivery. In the current work, we report on the fabrication of amphiphilic A2(BC)2 miktoarm poly(ϵ-caprolactone)2-[poly(2-(diethylamino)ethyl
check details methacrylate)-b-poly(poly (ethylene glycol) methyl ether methacrylate)]2 [(PCL)2(PDEA-b-PPEGMA)2] polymeric micelles as an integrated platform for intracellular delivery of the anticancer drug doxorubicin (Figure 1). Miktoarm star polymers (PCL)2(PDEA-b-PPEGMA)2 were synthesized by using the difunctional initiator for sequential ring opening polymerization (ROP) of ϵ-CL and continuous activators regenerated by electron transfer atom transfer radical polymerization (ARGET ATRP) of DEA and PEGMA. In aqueous solution, (PCL)2(PDEA-b-PPEGMA)2 could exist as structurally stable micelles possessing a hydrophobic PCL inner core, a Selleckchem XMU-MP-1 pH-sensitive PDEA middle layer, and a hydrophilic PPEGMA outer shell. The pH-responsive PDEA layer is hydrophobic and collapses on the core at the physiological pH (7.4)
which can prevent the premature burst drug release, but it becomes highly positively charged by protonation of the pendant tertiary amine groups and could lead the micelles to be adsorbed onto negatively charged cell membranes and C59 wnt nmr subsequently endocytosed by tumor cells at tumor extracellular pH. Once internalized and transferred to a lysosome, the further charged PDEA can lead to faster release of the entrapped drug into the cytoplasm and nucleus . Anti-tumor activities and intracellular uptake of drug-loaded (PCL)2(PDEA-b-PPEGMA)2 micelles were also investigated. Figure 1 Illustration of DOX-loaded (PCL) 2 (PDEA- b -PPEGMA) 2 micelles formation and intracellular DOX delivery triggered by endosomal GBA3 pH (pH 5.0). Methods Materials Pentaerythritol was dried under reduced pressure overnight prior to use. ϵ-Caprolactone (ϵ-CL, 99%,
Aldrich, St. Louis, MO, USA) was dried over calcium hydride and distilled under reduced pressure before use. 2-(Diethylamino)ethyl methacrylate (DEA, TCI-EP) was distilled from calcium hydride and stored under argon at −20°C. Poly(ethylene glycol) methyl ether methacrylate (PEGMA, M n = 475 Da, 99%, Aldrich) was purified by passing through a column filled with neutral alumina to remove inhibitor. Tetrahydrofuran (THF) was dried over sodium using benzophenone as a dryness indicator and distilled under nitrogen prior to use. Toluene was distilled from calcium hydride. Doxorubicin hydrochloride (DOX∙HCl) was purchased from Beijing Huafeng United Technology Co., Ltd., Beijing, China. Dulbecco’s modified Eagle medium (DMEM), fetal bovine serum (FBS), penicillin, and streptomycin were all purchased from Invitrogen, Carlsbad, CA, USA. HepG2 cells were purchased from the American Type Culture Collection (ATCC), Manassas, VA, USA, and cultured under the recommended conditions according to the supplier.