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Title Authors PubMed ID
1 Longhorn beetles (Coleoptera: Cerambycidae) community composition around different boreal infrastructures Noor S; Despland E; Montoro Girona M; Work T; 41638151
BIOLOGY
2 Scalable Synthesis of High-Quality Graphene Quantum Dots by Reductive Intercalation/Exfoliation of Coal Bepete G; Ratnayake G; Sanchez DE; Yu Z; Dimitrov E; Fest Carreno A; Oliveira MCD; Viana BC; Santos FEP; Terrones M; 41081673
PHYSICS
3 Upconversion Lanthanide-Based 2D Metal-Organic Frameworks for Multimode Information Encryption Chen J; Xie Y; Yang W; Sun R; Xing F; Mandl GA; Capobianco JA; Sun L; 40557752
CNSR
4 Non-invasive paper-based sensors containing rare-earth-doped nanoparticles for the detection of D-glucose López-Peña G; Ortiz-Mansilla E; Arranz A; Bogdan N; Manso-Silván M; Martín Rodríguez E; 38729020
CHEMBIOCHEM
5 Combining Pr3+-Doped Nanoradiosensitizers and Endogenous Protoporphyrin IX for X-ray-Mediated Photodynamic Therapy of Glioblastoma Cells Mandl GA; Vettier F; Tessitore G; Maurizio SL; Bietar K; Stochaj U; Capobianco JA; 37267436
CHEMBIOCHEM
6 Cooperative Sensitization Upconversion in Solution Dispersions of Co-Crystal Assemblies of Mononuclear Yb3+ and Eu3+ Complexes Sun G; Xie Y; Wang Y; Mandl GA; Maurizio SL; Zhang H; Ottenwaelder X; Capobianco JA; Sun L; 37040148
CNSR
7 Upconversion Luminescence through Cooperative and Energy-Transfer Mechanisms in Yb3+ -Metal-Organic Frameworks Xie Y; Sun G; Mandl GA; Maurizio SL; Chen J; Capobianco JA; Sun L; 36437239
CNSR
8 A Synthetic Biosensor for Detecting Putrescine in Beef Samples Selim AS; Perry JM; Nasr MA; Pimprikar JM; Shih SCC; 36356104
BIOLOGY
9 Energy migration control of multi-modal emissions in an Er3+ doped nanostructure toward information encryption and deep learning decoding Song Y; Lu M; Mandl GA; Xie Y; Sun G; Chen J; Liu X; Capobianco JA; Sun L; 34476872
ENCS
10 Direct Polymerization Approach to Synthesize Acid-Degradable Block Copolymers Bearing Imine Pendants for Tunable pH-Sensitivity and Enhanced Release. Hu X, Oh JK 32964550
CHEMBIOCHEM
11 The Key Role of Intrinsic Lifetime Dynamics from Upconverting Nanosystems in Multiemission Particle Velocimetry Tessitore G; Maurizio SL; Sabri T; Skinner CD; Capobianco JA; 32924221
CNSR
12 Optically Stimulated Nanodosimeters with High Storage Capacity. Van der Heggen D, Cooper DR, Tesson M, Joos JJ, Seuntjens J, Capobianco JA, Smet PF 31387200
CNSR

 

Title:Direct Polymerization Approach to Synthesize Acid-Degradable Block Copolymers Bearing Imine Pendants for Tunable pH-Sensitivity and Enhanced Release.
Authors:Hu XOh JK
Link:https://www.ncbi.nlm.nih.gov/pubmed/32964550
DOI:10.1002/marc.202000394
Publication:Macromolecular rapid communications
Keywords:acid-responsive degradationamphiphilic block copolymersenhanced/controlled drug releaseiminesnanoassembliesreversible addition fragmentation chain transfer polymerizationstimuli-responsive degradation
PMID:32964550 Category:Macromol Rapid Commun Date Added:2020-09-24
Dept Affiliation: CHEMBIOCHEM
1 Department of Chemistry and Biochemistry, Concordia University, H4B 1R6, Montreal, Quebec, Canada.

Description:

Direct Polymerization Approach to Synthesize Acid-Degradable Block Copolymers Bearing Imine Pendants for Tunable pH-Sensitivity and Enhanced Release.

Macromol Rapid Commun. 2020 Sep 22; :e2000394

Authors: Hu X, Oh JK

Abstract

The development of effective approaches to synthesize smart amphiphilic block copolymers (ABPs) exhibiting acid-responsive degradation through the cleavage of acid-labile imine bonds is extensively explored for controlled release of encapsulated biomolecules, particularly in drug delivery. Here, a new approach based on direct polymerization utilizing a controlled radical polymerization technique to synthesize acid-degradable ABPs bearing pendant imine linkages in hydrophobic block is reported. The approach centers on the synthesis of a novel methacrylate bearing benzoic imine group that can be polymerized to form the hydrophobic imine pendant block. The formed ABPs respond to mild acidic pHs equivalent to tumoral and endosomal/lysosomal acidic environments. This causes the dissociation of self-assembled nanoassemblies through change in their hydrophilic/hydrophobic balance upon the cleavage of pendant imine linkages to the corresponding aldehyde and primary amine, thus leading to the enhanced release of encapsulated drugs. The proof-of-concept results suggest that this robust approach is versatile to further design advanced nanoassemblies responding to dual/multiple stimuli, thus being more effective to intracellular drug delivery.

PMID: 32964550 [PubMed - as supplied by publisher]





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