Disulfide bond bridge insertion turns hydrophobic anticancer prodrugs into self-assembled nanomedicines
about
Tunable self-assembly of Irinotecan-fatty acid prodrugs with increased cytotoxicity to cancer cells.Self-Assembly of Amphiphilic Drug-Dye Conjugates into Nanoparticles for Imaging and Chemotherapy.A self-assembling nanomedicine of conjugated linoleic acid-paclitaxel conjugate (CLA-PTX) with higher drug loading and carrier-free characteristic.A facile route to form self-carried redox-responsive vorinostat nanodrug for effective solid tumor therapyDocetaxel prodrug liposomes for tumor therapy: characterization, in vitro and in vivo evaluation.Design and synthesis of theranostic antibiotic nanodrugs that display enhanced antibacterial activity and luminescence.Self-Assembled Redox Dual-Responsive Prodrug-Nanosystem Formed by Single Thioether-Bridged Paclitaxel-Fatty Acid Conjugate for Cancer Chemotherapy.A Nanosystem of Amphiphilic Oligopeptide-Drug Conjugate Actualizing Both αvβ3 Targeting and Reduction-Triggered Release for Maytansinoid.Bioreducible Hydrophobin-Stabilized Supraparticles for Selective Intracellular Release.Cancer Nanomedicines Stabilized by π-π Stacking between Heterodimeric Prodrugs Enable Exceptionally High Drug Loading Capacity and Safer Delivery of Drug Combinations.Facile Fabrication of Tumor Redox-Sensitive Nanoassemblies of Small-Molecule Oleate Prodrug as Potent Chemotherapeutic Nanomedicine.Rational Design of a New Self-Codelivery System from Redox-Sensitive Camptothecin-Cytarabine Conjugate Assembly for Effectively Synergistic Anticancer Therapy.Redox-responsive PEGylated self-assembled prodrug-nanoparticles formed by single disulfide bond bridge periplocymarin-vitamin E conjugate for liver cancer chemotherapy.Nanoprodrug of retinoic acid-modified paclitaxel.Gemcitabine-camptothecin conjugates: a hybrid prodrug for controlled drug release and synergistic therapeutics.Self-delivering prodrug-nanoassemblies fabricated by disulfide bond bridged oleate prodrug of docetaxel for breast cancer therapy.Construction and cellular uptake behavior of redox-sensitive docetaxel prodrug-loaded liposomes.Bioresponsive albumin-conjugated paclitaxel prodrugs for cancer therapy.Self-Assembly of Porphyrin-Paclitaxel Conjugates Into Nanomedicines: Enhanced Cytotoxicity due to Endosomal Escape.A dual-responsive nanocapsule via disulfide-induced self-assembly for therapeutic agent delivery.
P2860
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P2860
Disulfide bond bridge insertion turns hydrophobic anticancer prodrugs into self-assembled nanomedicines
description
2014 nî lūn-bûn
@nan
2014 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Disulfide bond bridge insertio ...... o self-assembled nanomedicines
@ast
Disulfide bond bridge insertio ...... o self-assembled nanomedicines
@en
type
label
Disulfide bond bridge insertio ...... o self-assembled nanomedicines
@ast
Disulfide bond bridge insertio ...... o self-assembled nanomedicines
@en
prefLabel
Disulfide bond bridge insertio ...... o self-assembled nanomedicines
@ast
Disulfide bond bridge insertio ...... o self-assembled nanomedicines
@en
P2093
P2860
P356
P1433
P1476
Disulfide bond bridge insertio ...... o self-assembled nanomedicines
@en
P2093
Guimei Lin
Hongjuan Zhang
Linxiang Zhao
Matthew T Haynes
Qiang Zhao
Qingchuan Zheng
P2860
P304
P356
10.1021/NL502044X
P407
P577
2014-09-07T00:00:00Z