Block ionomer micellar nanoparticles from double hydrophilic copolymers, classifications and promises for delivery of cancer chemotherapeutics

被引:30
作者
Abolmaali, S. S. [1 ]
Tamaddon, A. M. [2 ]
Salmanpour, M. [2 ]
Mohammadi, S. [2 ]
Dinarvand, R. [3 ]
机构
[1] Shiraz Univ Med Sci, Pharmaceut Nanotechnol Dept, Shiraz 71345, Iran
[2] Shiraz Univ Med Sci, Ctr Nanotechnol Drug Delivery, Shiraz 71345, Iran
[3] Univ Tehran Med Sci, Fac Pharm, Nanotechnol Res Ctr, Tehran 14174, Iran
关键词
Block ionomer; Double hydrophilic polymer; Micellar nanoparticles; Chemotherapeutic agents; Drug delivery; POLYION COMPLEX MICELLES; CROSS-LINKED MICELLES; POLYMERIC MICELLES; DRUG-DELIVERY; ANTITUMOR-ACTIVITY; CO-DELIVERY; PHOTODYNAMIC THERAPY; GRAFT COPOLYMER; IONIC CORES; PACLITAXEL;
D O I
10.1016/j.ejps.2017.04.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A class of double hydrophilic copolymers comprising ionic and nonionic water-soluble blocks, which are also called block ionomers, represent an interesting type of polymer assembly forming stable, homogeneous core corona dispersions. They exhibit the solution behavior of normal polyelectrolytes, whereas assembly into micelle, vesicle or disk morphology happens by an external stimulus (pH, temperature or ionic strength) or complex formation with metal ions, ionic surfactants, polyelectrolytes, etc. Temperature, pH, redox or salt sensitivity affords a unique opportunity to control the triggered release of payloads accommodated through electrostatic interaction, coordination or chemical conjugation. Moreover, the non-ionic block provides the surface passivation, prolongation of the blood circulation and tumor accumulation, supporting targeted delivery of chemotherapeutic agents based on pathophysiology of tumor microenvironment. Potentiation of antitumor activity, sensitization of the resistant tumors, increased tolerated dose and translation into clinical practice are among their most intriguing characteristics. Their high functionality has been suggested for co-delivery of multiple agents for reversal of chemo-resistance as well as simultaneous therapy and diagnostics. Nevertheless, some stability concerns may be raised due to the polymer disassembly beyond a critical concentration of pH, salt and polyion concentration that can be modulated by introducing crosslinks between the polymer chains (Nano-networks).
引用
收藏
页码:393 / 405
页数:13
相关论文
共 116 条
[31]  
Harada A., 1995, MACROMOLECULES, V28, P235
[32]   NC-6301, a polymeric micelle rationally optimized for effective release of docetaxel, is potent but is less toxic than native docetaxel in vivo [J].
Harada, Mitsunori ;
Iwata, Caname ;
Saito, Hiroyuki ;
Ishii, Kenta ;
Hayashi, Tatsuyuki ;
Yashiro, Masakazu ;
Hirakawa, Kosei ;
Miyazono, Kohei ;
Kato, Yasuki ;
Kano, Mitsunobu R. .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2012, 7 :2713-2727
[33]   Improved anti-tumor activity of stabilized anthracycline polymeric micelle formulation, NC-6300 [J].
Harada, Mitsunori ;
Bobe, Iulian ;
Saito, Hiroyuki ;
Shibata, Naoya ;
Tanaka, Ryosuke ;
Hayashi, Tatsuyuki ;
Kato, Yasuki .
CANCER SCIENCE, 2011, 102 (01) :192-199
[34]   Water-soluble nanospheres of poly(2-cinnamoylethyl methacrylate)-block-poly(acrylic acid) [J].
Henselwood, F ;
Liu, GJ .
MACROMOLECULES, 1997, 30 (03) :488-493
[35]   pH-responsive and charge shielded cationic micelle of poly(L-histidine)-block-short branched PEI for acidic cancer treatment [J].
Hu, Jun ;
Miura, Seiji ;
Na, Kun ;
Bae, You Han .
JOURNAL OF CONTROLLED RELEASE, 2013, 172 (01) :69-76
[36]   Characteristics of cancer cell death after exposure to cytotoxic drugs in vitro [J].
Huschtscha, LI ;
Bartier, WA ;
Ross, CEA ;
Tattersall, MHN .
BRITISH JOURNAL OF CANCER, 1996, 73 (01) :54-60
[37]   Clinical and electrophysiologic correlates of IVIg responsiveness in CIDP [J].
Iijima, M ;
Yamamoto, M ;
Hirayama, M ;
Tanaka, F ;
Katsuno, M ;
Mori, K ;
Koike, H ;
Hattori, N ;
Arimura, K ;
Nakagawa, M ;
Yoshikawa, H ;
Hayasaka, K ;
Onodera, O ;
Baba, M ;
Yasuda, H ;
Saito, T ;
Nakazato, M ;
Nakashima, K ;
Kira, J ;
Kaji, R ;
Oka, N ;
Sobue, G .
NEUROLOGY, 2005, 64 (08) :1471-1475
[38]   Polyion complex micelles for photodynamic therapy: Incorporation of dendritic photosensitizer excitable at long wavelength relevant to improved tissue-penetrating property [J].
Jang, Woo-Dong ;
Nakagishi, Yoshinori ;
Nishiyama, Nobuhiro ;
Kawauchi, Satoko ;
Morimoto, Yuji ;
Kikuchi, Makoto ;
Kataoka, Kazunori .
JOURNAL OF CONTROLLED RELEASE, 2006, 113 (01) :73-79
[39]   Multifunctional polymeric micelles for delivery of drugs and siRNA [J].
Jhaveri, Aditi M. ;
Torchilin, Vladimir P. .
FRONTIERS IN PHARMACOLOGY, 2014, 5
[40]   Polymer genomics: An insight into pharmacology and toxicology of nanomedicines [J].
Kabanov, Alexander V. .
ADVANCED DRUG DELIVERY REVIEWS, 2006, 58 (15) :1597-1621