Photoreduction of Self-Assembled Lipidporphyrinato-iron(III) Chloride with Hyaluronic Acid under Semi-Physiological Conditions

2000 ◽  
Vol 29 (1) ◽  
pp. 84-85
Author(s):  
Teruyuki Komatsu ◽  
Tetsuya Yanagimoto ◽  
Akito Nakagawa ◽  
Eishun Tsuchida
Biomaterials ◽  
2021 ◽  
pp. 120967
Author(s):  
Li-Jung Kang ◽  
Juhwan Yoon ◽  
Jun Gi Rho ◽  
Hwa Seung Han ◽  
Seulbi Lee ◽  
...  

2018 ◽  
Vol 16 (1) ◽  
pp. 128-140 ◽  
Author(s):  
Hibah M Aldawsari ◽  
Harkiranpreet Kaur Dhaliwal ◽  
Bader Mubarak Aljaeid ◽  
Nabil A. Alhakamy ◽  
Zainy Mohammad Banjar ◽  
...  

Biomolecules ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1478
Author(s):  
Tatiana Guzzo ◽  
Fabio Barile ◽  
Cecilia Marras ◽  
Davide Bellini ◽  
Walter Mandaliti ◽  
...  

The stability and the degradation of polymers in physiological conditions are very important issues in biomedical applications. The copolymer of hyaluronic acid and poly-D,L-lactic acid (made available in a product called DAC®) produces a hydrogel which retains the hydrophobic character of the poly-D,L-lactide sidechains and the hydrophilic character of a hyaluronic acid backbone. This hydrogel is a suitable device for the coating of orthopedic implants with structured surfaces. In fact, this gel creates a temporary barrier to bacterial adhesion by inhibiting colonization, thus preventing the formation of the biofilm and the onset of an infection. Reabsorbed in about 72 h after the implant, this hydrogel does not hinder bone growth processes. In the need to assess stability and degradation of both the hyaluronan backbone and of the polylactic chains along time and temperature, we identified NMR spectroscopy as a privileged technique for the characterization of the released species, and we applied diffusion-ordered NMR spectroscopy (DOSY-NMR) for the investigation of molecular weight dispersion. Our diffusion studies of DAC® in physiological conditions provided a full understanding of the product degradation by overcoming the limitations observed in applying classical chromatography approaches by gel permeation UV.


Biomaterials ◽  
2010 ◽  
Vol 31 (1) ◽  
pp. 106-114 ◽  
Author(s):  
Ki Young Choi ◽  
Hyunjin Chung ◽  
Kyung Hyun Min ◽  
Hong Yeol Yoon ◽  
Kwangmeyung Kim ◽  
...  

Biomaterials ◽  
2012 ◽  
Vol 33 (7) ◽  
pp. 2310-2320 ◽  
Author(s):  
Jing Li ◽  
Meirong Huo ◽  
Jing Wang ◽  
Jianping Zhou ◽  
Jumah M. Mohammad ◽  
...  

2019 ◽  
Vol Volume 14 ◽  
pp. 8195-8208 ◽  
Author(s):  
Yeon-Ju Kim ◽  
Haribalan Perumalsamy ◽  
Verónica Castro-Aceituno ◽  
Donghyuk Kim ◽  
Josua Markus ◽  
...  

2009 ◽  
Vol 19 (24) ◽  
pp. 4102 ◽  
Author(s):  
Ki Young Choi ◽  
Kyung Hyun Min ◽  
Jin Hee Na ◽  
Kuiwon Choi ◽  
Kwangmeyung Kim ◽  
...  

2010 ◽  
Vol 2010 ◽  
pp. 1-9 ◽  
Author(s):  
Xuemeng Dong ◽  
Chenguang Liu

Novel amphiphilic biopolymers were synthesized using hyaluronic acid (HA) as a hydrophilic segment and deoxycholic acid (DOCA) as a hydrophobic segment by a 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide mediated coupling reaction. The structural characteristics of the HA-DOCA conjugates were investigated usingH1NMR. Self-assembled nanoparticles were prepared based on HA-DOCA conjugates, and its characteristics were investigated using dynamic laser light scattering, transmission electron microscopy (TEM), and fluorescence spectroscopy. The mean diameter was about 293.5 nm with unimodal size distribution in distilled water. The TEM images revealed that the shape of HA-DOCA self-aggregates was spherical. The critical aggregation concentration (CAC) was in the range of 0.025–0.056 mg/mL. The partition equilibrium constant (Kv) of pyrene in self-aggregates solution was from1.45×104to3.64×104. The aggregation number of DOCA groups per hydrophobic microdomain, estimated by the fluorescence quenching method using cetylpyridinium chloride, increased with increasing degree of substitution.


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