Ultrasound-degradable serum albumin nanoplatform for in situ controlled drug release

2020 ◽  
Vol 56 (54) ◽  
pp. 7503-7506
Author(s):  
Jianjun Du ◽  
Yu Zhang ◽  
Haoying Ge ◽  
Chao Shi ◽  
Saran Long ◽  
...  

An ultrasound-modulated drug release nanoplatform was fabricated using a degradable azo derivative (ACVA) as a crosslinker for excellent tissue penetration, and could realize controllable drug release according to the treatment needs.

2019 ◽  
Vol 10 (5) ◽  
pp. 1401-1409 ◽  
Author(s):  
Yufu Tang ◽  
Xiaomei Lu ◽  
Chao Yin ◽  
Hui Zhao ◽  
Wenbo Hu ◽  
...  

Tissue-penetration-depth-independent self-luminescence is highly expected to perform photoisomerization-related bioapplications in vivo to overcome the limitation of shallow tissue-penetration from external photoexcitation.


1998 ◽  
Vol 51 (1) ◽  
pp. 23-34 ◽  
Author(s):  
G. Imanidis ◽  
S. Helbing-Strausak ◽  
R. Imboden ◽  
H. Leuenberger

ACS Nano ◽  
2014 ◽  
Vol 9 (1) ◽  
pp. 789-798 ◽  
Author(s):  
Penghui Zhang ◽  
Zhimei He ◽  
Chen Wang ◽  
Jiangning Chen ◽  
Jingjing Zhao ◽  
...  

Pharmaceutics ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 969
Author(s):  
Marzia Cirri ◽  
Francesca Maestrelli ◽  
Giulia Nerli ◽  
Natascia Mennini ◽  
Mario D’Ambrosio ◽  
...  

A thermosensitive, mucoadhesive in-situ gel for clonazepam (CLZ) intranasal delivery was developed, which aimed to achieve prolonged in-situ residence and controlled drug release, overcoming problems associated with its oral or parenteral administration. Poloxamer was selected as a thermosensitive polymer and chitosan glutamate and sodium hyaluronate as mucoadhesive and permeation enhancer. Moreover, randomly methylated β-Cyclodextrin (RAMEB) was used to improve the low drug solubility. A screening DoE was applied for a systematic examination of the effect of varying the formulation components proportions on gelation temperature, gelation time and pH. Drug-loaded gels at different clonazepam-RAMEB concentrations were then prepared and characterized for gelation temperature, gelation time, gel strength, mucoadhesive strength, mucoadhesion time, and drug release properties. All formulations showed suitable gelation temperature (29–30.5 °C) and time (50–65 s), but the one with the highest drug-RAMEB concentration showed the best mucoadhesive strength, longest mucoadhesion time (6 h), and greatest release rate. Therefore, it was selected for cytotoxicity and permeation studies through Caco-2 cells, compared with an analogous formulation without RAMEB and a drug solution. Both gels were significantly more effective than the solution. However, RAMEB was essential not only to promote drug release, but also to reduce drug cytotoxicity and further improve its permeability.


2019 ◽  
Vol 2 (2) ◽  
pp. 263-272
Author(s):  
Yuping Liu ◽  
Guiying Kang ◽  
Lu Sun ◽  
Chao Meng ◽  
Jinlei Peng ◽  
...  

2016 ◽  
Vol 59 (11) ◽  
pp. 892-900 ◽  
Author(s):  
Malathi Mathiyazhakan ◽  
Paul Kumar Upputuri ◽  
Kathyayini Sivasubramanian ◽  
Ashish Dhayani ◽  
Praveen Kumar Vemula ◽  
...  

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