4.8 Article

Dendrimer-decorated nanogels: Efficient nanocarriers for biodistribution in vivo and chemotherapy of ovarian carcinoma

期刊

BIOACTIVE MATERIALS
卷 6, 期 10, 页码 3244-3253

出版社

KEAI PUBLISHING LTD
DOI: 10.1016/j.bioactmat.2021.02.031

关键词

Nanogels; Dendrimer; Surface charge; Thermal/pH dual-responsiveness; Drug delivery

资金

  1. Sino-German Center for Research Promotion [GZ1505]
  2. DFG [SFB 985]
  3. National Natural Science Foundation of China [81801704, 81761148028]
  4. Science and Technology Commission of Shanghai Municipality [18520750400]
  5. Shanghai Sailing Program [18YF1415300]
  6. China Scholarship Council

向作者/读者索取更多资源

Novel PVCL-GMA nanogels decorated with PAMAM dendrimers were developed, exhibiting a unique structure with GMA-rich domains localized on the surface. The modification of overall charge to positive by G2 dendrimer decoration resulted in improved biodistribution, reduced liver accumulation, enhanced tumor uptake, and promoted drug release in vivo, leading to significantly augmented antitumor efficacy with low side effects.
Nanomedicine has revolutionized disease theranostics by the accurate diagnosis and efficient therapy. Here, the PAMAM dendrimer decorated PVCL-GMA nanogels (NGs) were developed for favorable biodistribution in vivo and enhanced antitumor efficacy of ovarian carcinoma. By an ingenious design, the NGs with a unique structure that GMA-rich domains were localized on the surface were synthesized via precipitation polymerization. After G2 dendrimer decoration, the overall charge is changed from neutral to positive, and the NGs-G2 display the whole charge nature of positively charged corona and neutral core. Importantly, the unique architecture and charge conversion of NGs-G2 have a profound impact on the biodistribution and drug delivery in vivo. As a consequence of this alteration, the NGs-G2 as nanocarriers emerge the highly sought biodistribution of reduced liver accumulation, enhanced tumor uptake, and promoted drug release, resulting in the significantly augmented antitumor efficacy with low side effects. Remarkably, this finding is contrary to some reported work that the nanocarriers with positive charge have preferential liver uptake. Moreover, the NGs-G2 also displayed thermal/ pH dual-responsive behaviors, excellent biocompatibility, improved cellular uptake, and stimuli-responsive drug release. Encouragingly, this work demonstrates a novel insight into the strategy for optimizing design, improving biodistribution and enhancing theranostic efficacy of nanocarriers.

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