Literature DB >> 31837355

Length effect of stimuli-responsive block copolymer prodrug filomicelles on drug delivery efficiency.

Wendong Ke1, Nannan Lu2, Abd Al-Wali Mohammed M Japir1, Qinghao Zhou1, Longchang Xi1, Yuheng Wang1, Debabrata Dutta1, Min Zhou3, Yueyin Pan2, Zhishen Ge4.   

Abstract

Filomicelles possess some unique properties for improved in vivo drug delivery efficiency relative to commonly used spherical nanocarriers, which have attracted great interests. However, the length effect of the block copolymer prodrug-based filomicelles with a comparable cross-section diameter on the drug delivery efficiency and antitumor efficacy still need to be systematically studied. In this report, we prepare three optimized nanoparticles with a comparable cross-section diameter of ~40 nm, including long filomicelles (LFMs) with the length of ~2.5 μm, short filomicelles (SFMs) with the length of ~180 nm, and spherical micelles (SMs) with a diameter of ~40 nm. All of them are self-assembled from the pH and oxidation dual-responsive block copolymer prodrug, PEG-b-P(CPTKMA-co-PEMA), consisting of poly(ethylene glycol) (PEG) and a copolymerized block of thioketal-linked camptothecin methacrylate (CPTKMA) and 2-(pentamethyleneimino) ethyl methacrylate (PEMA). At pH 6.5, the nanoparticles are positively charged due to the protonation of PPEMA segments. Among them, SFMs are demonstrated to be internalized into cells most efficiently at pH 6.5 due to larger interaction areas with cell membranes relative to SMs. Moreover, SFMs show prolonged blood circulation similar to SMs as well as deepest tumor penetration and best antitumor efficacy among the three nanoparticles. LFMs show worst in vivo performance because their too long structure limits the cellular uptake and tumor accumulation. Therefore, the responsive polymer prodrug filomicelles with an optimized length show great potentials to overcome the physiological barriers and improve the drug delivery efficiency.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Anticancer drug delivery; Block copolymer prodrug; Filomicelle; Nanoparticle shape; Responsive drug release

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Substances:

Year:  2019        PMID: 31837355     DOI: 10.1016/j.jconrel.2019.12.012

Source DB:  PubMed          Journal:  J Control Release        ISSN: 0168-3659            Impact factor:   9.776


  3 in total

1.  Pi-stacking Enhances Stability, Scalability of Formation, Control over Flexibility and Circulation Time of Polymeric Filaments.

Authors:  Sophia Li; Sharan Bobbala; Michael P Vincent; Mallika Modak; Yugang Liu; Evan A Scott
Journal:  Adv Nanobiomed Res       Date:  2021-08-05

2.  ROS-responsive chitosan-SS31 prodrug for AKI therapy via rapid distribution in the kidney and long-term retention in the renal tubule.

Authors:  Di Liu; Gaofeng Shu; Feiyang Jin; Jing Qi; Xiaoling Xu; Yan Du; Hui Yu; Jun Wang; Mingchen Sun; Yuchan You; Minxia Zhu; Meixuan Chen; Luwen Zhu; Qiying Shen; Xiaoying Ying; Xuefang Lou; Saiping Jiang; Yongzhong Du
Journal:  Sci Adv       Date:  2020-10-09       Impact factor: 14.136

Review 3.  Bioresponsive drug delivery systems for the treatment of inflammatory diseases.

Authors:  Yin Dou; Chenwen Li; Lanlan Li; Jiawei Guo; Jianxiang Zhang
Journal:  J Control Release       Date:  2020-09-08       Impact factor: 9.776

  3 in total

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