2015
DOI: 10.1016/j.polymer.2015.01.067
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Diblock copolymer micelles as surface-functionalized particles and direct decoration of nanoparticles on their surface

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Cited by 6 publications
(4 citation statements)
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“…'Smart' drug delivery systems have attracted much interest from pharmacologists and biomaterials scientists in previous decades, and amphiphilic polymers with the ability to selfassemble into micelles in aqueous solutions are highly promising. [1][2][3][4] Advantages of using polymeric micelles as drug carriers include relatively easy structural and functional modication, improved biodistribution and bioavailability of the drugs, and targeted delivery of drugs to correct locations such as tumor cells. [5][6][7][8] As most anticancer drugs have poor solubility, high side effects and low bioavailability, the encapsulation of anticancer drugs in polymeric micelles could not only improve the solubility of drugs, but also decrease the risk of multidrug resistance.…”
Section: Introductionmentioning
confidence: 99%
“…'Smart' drug delivery systems have attracted much interest from pharmacologists and biomaterials scientists in previous decades, and amphiphilic polymers with the ability to selfassemble into micelles in aqueous solutions are highly promising. [1][2][3][4] Advantages of using polymeric micelles as drug carriers include relatively easy structural and functional modication, improved biodistribution and bioavailability of the drugs, and targeted delivery of drugs to correct locations such as tumor cells. [5][6][7][8] As most anticancer drugs have poor solubility, high side effects and low bioavailability, the encapsulation of anticancer drugs in polymeric micelles could not only improve the solubility of drugs, but also decrease the risk of multidrug resistance.…”
Section: Introductionmentioning
confidence: 99%
“…A method was proposed to improve the interface adhesion strength between the filler and the matrix of composite material by modifying the interface with catechol groups and coupling agents. [16,[40][41]42,43] At first, polydopamine (PDA) was formed by using dopamine self-polymerization functionalize BN and then dopamine-modified BN (DBN) was obtained in an alkaline environment. [44,45] After that, the secondary modification was performed, and the DBN was modified by an epoxy-functionalized silane coupling agent (KH-560) to obtain k-DBN.…”
Section: Introductionmentioning
confidence: 99%
“…16 Dopamine-functionalized diBCPs, 17,18 such as poly(dopamine acrylamide)-b-polystyrene (PDA-b-PS) have also been synthesized. 18 For the tailoring of surface or interfacial properties of BCPs, the combination of architecture and reactive functionalities appears to be an ideal approach. The PEO-b-PLA BCPs containing a small quantity of carboxylic acid in the PLA block were synthesized.…”
Section: Introductionmentioning
confidence: 99%
“…A amphiphilic diBCP which bears reactive trimethoxysilane groups in one segment was prepared and used as the precursor of the hybrid vesicle . Dopamine‐functionalized diBCPs, such as poly(dopamine acrylamide)‐ b ‐polystyrene (PDA‐ b ‐PS) have also been synthesized …”
Section: Introductionmentioning
confidence: 99%