In-Solution Structural Considerations by1H NMR and Solid-State Thermal Properties of Inulin-d-α-Tocopherol Succinate (INVITE) Micelles as Drug Delivery Systems for Hydrophobic Drugs

2014 ◽  
Vol 215 (21) ◽  
pp. 2084-2096 ◽  
Author(s):  
Laura Catenacci ◽  
Delia Mandracchia ◽  
Milena Sorrenti ◽  
Lino Colombo ◽  
Massimo Serra ◽  
...  
Author(s):  
Naveed Ahmed ◽  
C.E. Mora-Huertas ◽  
Chiraz Jaafar-Maalej ◽  
Hatem Fessi ◽  
Abdelhamid Elaissari

2021 ◽  
pp. 129-164
Author(s):  
Ankita Banerjee ◽  
Rajesh Kumar ◽  
Monica Gulati ◽  
Sachin Kumar Singh ◽  
Kamal Dua ◽  
...  

2020 ◽  
Vol 153 (15) ◽  
pp. 154506
Author(s):  
Benjamin Malfait ◽  
Natália T. Correia ◽  
Carmen Ciotonea ◽  
Jérémy Dhainaut ◽  
Jean-Philippe Dacquin ◽  
...  

2016 ◽  
Vol 7 (4) ◽  
pp. 887-898 ◽  
Author(s):  
Stefano Stefani ◽  
Indah N. Kurniasih ◽  
Sunil K. Sharma ◽  
Christoph Böttcher ◽  
Paul Servin ◽  
...  

A set of biodegradable nanocarriers characterized by a hyperbranched polyester core and an amphiphilic branched shell was developed and employed to efficiently solubilize hydrophobic drugs in aqueous media.


2017 ◽  
Vol 8 (13) ◽  
pp. 2105-2114 ◽  
Author(s):  
Weizhi Chen ◽  
Shilu Ji ◽  
Xiaoping Qian ◽  
Yajun Zhang ◽  
Cheng Li ◽  
...  

Packaging hydrophobic drugs into nanoparticles can improve their aqueous solubility, tumor-specific accumulation and therapeutic effect.


2021 ◽  
Vol 903 ◽  
pp. 3-8
Author(s):  
Mārīte Skrinda ◽  
Arita Dubnika ◽  
Janis Locs

Liposomes are being used as unique drug delivery systems due to their ability to encapsulate both hydrophilic and hydrophobic drugs, as well as for the fact that they improve the disadvantages of free drug administration. However, liposomes have a significant disadvantage - low encapsulation efficiency. In the research carried out, 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC) and cholesterol (Chol), in the ratio (n/n) of 2:1, 3:1 and 4:1 respectively, were used to prepare the liposomes. Blank liposomes (LIP) and vancomycin hydrochloride (VANKA) containing liposomes (VANKA-LIP) were prepared for each of the DSPC and Chol compositions. The aim of our study was to evaluate the effect of liposome composition on the VANKA encapsulation efficiency and release kinetics.


2021 ◽  
Vol 43 (6) ◽  
pp. 645-645
Author(s):  
dil Karaca A ar dil Karaca A ar

Recently, polyurethane materials are widely used for many application areas such as drug delivery systems, biomaterial production, etc. In this study, polyurethane structures containing different amounts of gelatin (5%, 10%) were prepared. A release system was designed with ciprofloxacin adsorption to the prepared polyurethane structures. The structural characterization, thermal properties, surface morphologies of the designed system were determined using appropriate techniques. Monitoring of ciprofloxacin release was carried out by UV-spectrophotometer. It was determined that polyurethane structures containing different proportions of gelatin supported the adsorption of ciprofloxacin and the release slowed down with the increasing gelatin ratio. With this study, many drug delivery systems that can release at different rates and durations depending on the amount of gelatin additive can be designed.


2013 ◽  
Vol 6 (2) ◽  
pp. 355-362 ◽  
Author(s):  
Udaya Sakthi M. ◽  
Josephine Ritashinita Lobo F. ◽  
Kiran B. Uppuluri

Sign in / Sign up

Export Citation Format

Share Document