Synthesis and characterization of thermoresponsive polyamidoamine-polyethylene glycol-poly(D,L-lactide) core-shell nanoparticles.
Synthesis and characterization of thermoresponsive polyamidoamine-polyethylene glycol-poly(D,L-lactide) core-shell nanoparticles.
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DOI:
10.1016/j.actbio.2009.08.036
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发表时间:
2010-03
影响因子:
9.7
通讯作者:
Yang, Hu
中科院分区:
文献类型:
--
作者:
Kailasan, Arunvel;Yuan, Quan;Yang, Hu
This work describes the synthesis and characterization of novel thermoresponsive highly-branched polyamidoamine-polyethylene glycol-poly (D, L-lactide) (PAMAM-PEG-PDLLA) core-shell nanoparticles. A series of dendritic PEG-PDLLA nanoparticles were synthesized through conjugation of PEG of various chain lengths (1500, 6000, and 12000 g/mol) to polyamidoamine (PAMAM) dendrimer G3.0 and subsequent ring-opening polymerization of DLLA. Ninhydrin assay, 1H-NMR, FT-IR, dynamic light scattering, AFM were used to characterize the structure and compositions of dendritic PEG-PDLLA nanoparticles. Sol-gel phase transition of aqueous dendritic PEG-PDLLA solutions was measured using UV-Vis spectroscocopy. According to our results, dendritic PEG-PDLLA nanoparticles in aqueous solutions can self-assemble into sub-micron/micron aggregates and the size of aggregates is dependent on temperature and PEG-PDLLA chain length. Further, dendritic PEG-PDLLA solutions exhibit sol-gel phase transition with increasing temperature. The constructed dendritic PEG-PDLLA nanoparticles possess high cytocompatibility, which is significantly improved as compared to PAMAM dendrimers. The potential of dendritic PEG-PDLLA nanoparticles for encapsulation of water insoluble drugs such as camptothecin was demonstrated. Dendritic PEG-PDLLA nanoparticles we developed offer greater structural flexibility and provide a novel nanostructured thermoresponsive carrier for drug delivery.
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影响因子:
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通讯作者:
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