Zwitterionic shielded polymeric prodrug with folate-targeting and pH responsiveness for drug deliveryElectronic supplementary information (ESI) available: Experimental details and characterization data. 1H NMR and 13C NMR spectra of PEGMA-BZ monomer. 1H NMR spectra of 4-cyano-4-ethylsulfanylthiocarbonylsulfanylentanoic acid (CEP) and folic acid. 31P spectrum of P(MPC-co-PEGMA-BZ) copolymer. UV-vis spectra of (A) P(MPC-co-PEGMA-BZ)-g-DOX prodrug, (B) P(MPC-co-PEGMA-BZ), and (C) the reaction produ

Zwitterionic polymers are a class of polymers that acts as both Lewis base and Lewis acid in solution. These polymers not only have excellent properties of hydration, anti-bacterial adhesion, charge reversal and easy chemical modification, but also have characteristics of long-term circulation and s...

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Main Authors Li, Lei, Song, Yue, He, Jinlin, Zhang, Mingzu, Liu, Jian, Ni, Peihong
Format Journal Article
LanguageEnglish
Published 30.01.2019
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Summary:Zwitterionic polymers are a class of polymers that acts as both Lewis base and Lewis acid in solution. These polymers not only have excellent properties of hydration, anti-bacterial adhesion, charge reversal and easy chemical modification, but also have characteristics of long-term circulation and suppress nonspecific protein adsorption in vivo . Here, we describe a novel folate-targeted and acid-labile polymeric prodrug under the microenvironment of tumor cells, abbreviated as FA-P(MPC- co -PEGMA-BZ)- g -DOX, which was synthesized via a combination of reversible addition-fragmentation chain transfer (RAFT) copolymerization, Schiff-base reaction, Click chemistry, and a reaction between the amine group of doxorubicin (DOX) and aldehyde functionalities of P(MPC- co -PEGMA-BZ) pendants, wherein MPC and PEGMA-BZ represent 2-(methacryloyloxy)ethyl phosphorylcholine and polyethylene glycol methacrylate ester benzaldehyde, respectively. The polymeric prodrug could self-assemble into nanoparticles in an aqueous solution. The average particle size and morphologies of the prodrug nanoparticles were observed by dynamic light scattering (DLS) and transmission electron microscopy (TEM), respectively. We also investigated the in vitro drug release behavior and observed rapid prodrug nanoparticle dissociation and drug release under a mildly acidic microenvironment. The methyl thiazolyl tetrazolium (MTT) assay verified that the P(MPC- co -PEGMA-BZ) copolymer possessed good biocompatibility and the FA-P(MPC- co -PEGMA-BZ)- g -DOX prodrug nanoparticles showed higher cellular uptake than those prodrug nanoparticles without the FA moiety. The results of cytotoxicity and the intracellular uptake of non-folate/folate targeted prodrug nanoparticles further confirmed that FA-P(MPC- co -PEGMA-BZ)- g -DOX could be efficiently accumulated and rapidly internalized by HeLa cells due to the strong interaction between multivalent phosphorylcholine (PC) groups and cell membranes. This kind of multifunctional FA-P(MPC- co -PEGMA-BZ)- g -DOX prodrug nanoparticle with combined target-ability and pH responsiveness demonstrates promising potential for cancer chemotherapy. Zwitterionic polymers are a class of polymers that acts as both Lewis base and Lewis acid in solution.
Bibliography:13
C NMR spectra of PEGMA-BZ monomer.
g
PEGMA-BZ) with triethylamine. UV-vis spectra of free folate and FA-P(MPC-
I
co
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1
H NMR and
P spectrum of P(MPC-
10.1039/c8tb02772b
H NMR spectra of 4-cyano-4-ethylsulfanylthiocarbonylsulfanylentanoic acid (CEP) and folic acid.
3
DOX in ethanol. Intensity ratios
PEGMA-BZ), and (C) the reaction product of P(MPC-
as a function of Log C for (A) PMPD1 and (B) FA-PMPD1 prodrug nanoparticles in pH 7.4 buffer solution. TEM image of the PMPD1 prodrug nanoparticles (A) and the particle size distribution curve (B) corresponding to the TEM sample (scale bar 200 nm). Variation of particle size for the FA-PMPD1 prodrug nanoparticles in PBS 7.4 at different times. See DOI
PEGMA-BZ) copolymer. UV-vis spectra of (A) P(MPC-
Electronic supplementary information (ESI) available: Experimental details and characterization data.
DOX prodrug, (B) P(MPC-
31
PEGMA-BZ)-
ISSN:2050-750X
2050-7518
DOI:10.1039/c8tb02772b