Synthesis of pH-responsive photocrosslinked hyaluronic acid-based hydrogels for drug delivery

2012 ◽  
Vol 50 (17) ◽  
pp. 3507-3516 ◽  
Author(s):  
Youhua Tao ◽  
Ling Ai ◽  
Huiyu Bai ◽  
Xiaoya Liu
2019 ◽  
Vol 135 ◽  
pp. 240-247 ◽  
Author(s):  
Bingyang Lu ◽  
Dan Luo ◽  
Ansha Zhao ◽  
Haohao Wang ◽  
Yuancong Zhao ◽  
...  

2019 ◽  
Vol 55 (8) ◽  
pp. 1164-1167 ◽  
Author(s):  
Yu-Hui Zhang ◽  
Ying-Ming Zhang ◽  
Jie Yu ◽  
Jie Wang ◽  
Yu Liu

A polysaccharide nanoconjugate was fabricated from N-(2-aminoethyl)-gluconamide-grafted hyaluronic acid and bortezomib, displaying pH-responsive targeted drug release and higher anticancer effect.


2015 ◽  
Vol 3 (10) ◽  
pp. 1386-1394 ◽  
Author(s):  
Yanan Luo ◽  
Xuenv Wang ◽  
Dan Du ◽  
Yuehe Lin

In this paper, we proposed a naturally derived protein cage based pH-responsive delivery system for intracellular prodrug controlled release.


2020 ◽  
Vol 8 (7) ◽  
pp. 1885-1896 ◽  
Author(s):  
Xinyu Zhang ◽  
Minyi Zhao ◽  
Nan Cao ◽  
Wei Qin ◽  
Meng Zhao ◽  
...  

To improve the tumor cell active targeting, uptake efficiency and circulation time of doxorubicin (DOX) in vivo. Herein, we constructed a cleavable PEGylated hyaluronic acid nano-drug delivery system (HA–mPEG2k–DOX) based on pH-responsive imine bond.


Pharmaceutics ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 636 ◽  
Author(s):  
Jung Min Shin ◽  
Gwan Hyun Choi ◽  
Seok Ho Song ◽  
Hyewon Ko ◽  
Eun Sook Lee ◽  
...  

Although self-assembled nanoparticles (SNPs) have been used extensively for targeted drug delivery, their clinical applications have been limited since most of the drugs are released into the blood before they reach their target site. In this study, metal-phenolic network (MPN)-coated SNPs (MPN-SNPs), which consist of an amphiphilic hyaluronic acid derivative, were prepared to be a pH-responsive nanocarrier to facilitate drug release in tumor microenvironments (TME). Due to their amphiphilic nature, SNPs were capable of encapsulating doxorubicin (DOX), chosen as the model anticancer drug. Tannic acid and FeCl3 were added to the surface of the DOX-SNPs, which allowed them to be readily coated with MPNs as the diffusion barrier. The pH-sensitive MPN corona allowed for a rapid release of DOX and effective cellular SNP uptake in the mildly acidic condition (pH 6.5) mimicking TME, to which the hyaluronic acid was exposed to facilitate receptor-mediated endocytosis. The DOX-loaded MPN-SNPs exhibited a higher cytotoxicity for the cancer cells, suggesting their potential use as a drug carrier in targeted cancer therapy.


Pharmaceutics ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 247 ◽  
Author(s):  
Gyeong Jin Lee ◽  
Tae-il Kim

i-motif is cytosine (C)-rich oligonucleotide (ODN) which shows pH-responsive structure change in acidic condition. Therefore, it has been utilized for the trigger of intercalated drug release, responding to environmental pH change. In this study, 2.76 molecules of i-motif binding ODNs (IBOs) were conjugated to each hyaluronic acid (HA) via amide bond linkages. Synthesis of HA-IBO conjugate (HB) was confirmed by FT-IR and agarose gel electrophoresis with Stains-All staining. After hybridization of HB with i-motif ODN (IMO), it was confirmed that doxorubicin (DOX) could be loaded in HB-IMO hybrid structure (HBIM) with 65.6% of drug loading efficiency (DLE) and 25.0% of drug loading content (DLC). At pH 5.5, prompt and significant DOX release from HBIM was observed due to the disruption of HBIM hybrid structure via i-motif formation of IMO, contrary to pH 7.4 condition. Then, HBIM was complexed with low molecular weight polyethylenimine (PEI1.8k), forming positively charged nanostructures (Z-average size: 126.0 ± 0.4 nm, zeta-potential: 16.1 ± 0.3 mV). DOX-loaded HBIM/PEI complexes displayed higher anticancer efficacy than free DOX in A549 cells, showing the potential for pH-responsive anticancer drug delivery systems.


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