scholarly journals Immobilized thermolysin for highly efficient production of low-molecular-weight protamine-An attractive cell-penetrating peptide for macromolecular drug delivery applications

2011 ◽  
Vol 100A (1) ◽  
pp. 211-219 ◽  
Author(s):  
Allan E. David ◽  
Junbo Gong ◽  
Beata Chertok ◽  
Roman C. Domszy ◽  
Cheol Moon ◽  
...  
2010 ◽  
Vol 15 (23-24) ◽  
pp. 1109-1109
Author(s):  
Jacob A.D. Clausen ◽  
Lars Linderoth ◽  
Rikke Bjerring Andersen ◽  
Henrik Franzyk ◽  
Hanne M. Nielsen

2014 ◽  
Vol 193 ◽  
pp. 63-73 ◽  
Author(s):  
Huining He ◽  
Junxiao Ye ◽  
Ergang Liu ◽  
Qiuling Liang ◽  
Quan Liu ◽  
...  

Biomaterials ◽  
2010 ◽  
Vol 31 (6) ◽  
pp. 1429-1443 ◽  
Author(s):  
Young-Suk Choi ◽  
Jue Yeon Lee ◽  
Jin Sook Suh ◽  
Young-Min Kwon ◽  
Seung-Jin Lee ◽  
...  

Polymers ◽  
2021 ◽  
Vol 13 (23) ◽  
pp. 4078
Author(s):  
Cristina Gonzalez-Melo ◽  
Andres J. Garcia-Brand ◽  
Valentina Quezada ◽  
Luis H. Reyes ◽  
Carolina Muñoz-Camargo ◽  
...  

Gelatin and chitosan nanoparticles have been widely used in pharmaceutical, biomedical, and nanofood applications due to their high biocompatibility and biodegradability. This study proposed a highly efficient synthesis method for type B gelatin and low-molecular-weight (LMW) chitosan nanoparticles. Gelatin nanoparticles (GNPs) were synthesized by the double desolvation method and the chitosan nanoparticles (CNPs) by the ionic gelation method. The sizes of the obtained CNPs and GNPs (373 ± 71 nm and 244 ± 67 nm, respectively) and zeta potential (+36.60 ± 3.25 mV and −13.42 ± 1.16 mV, respectively) were determined via dynamic light scattering. Morphology and size were verified utilizing SEM and TEM images. Finally, their biocompatibility was tested to assure their potential applicability as bioactive molecule carriers and cell-penetrating agents.


RSC Advances ◽  
2016 ◽  
Vol 6 (24) ◽  
pp. 19751-19757 ◽  
Author(s):  
Siddhi Gupta ◽  
Manish Singh ◽  
Amarendar Reddy M. ◽  
Prabhu S. Yavvari ◽  
Aasheesh Srivastava ◽  
...  

We present the effect of size, charge, and hydrophobicity of anticancer drugs on their drug encapsulation efficacy in anl-alanine-based small-molecule hydrogelator.


2014 ◽  
Vol 25 (11) ◽  
pp. 1337-1341 ◽  
Author(s):  
Nhung Do ◽  
Günther Weindl ◽  
Emanuel Fleige ◽  
Mario Salwiczek ◽  
Beate Koksch ◽  
...  

2014 ◽  
Vol 12 (10) ◽  
pp. 1652-1663 ◽  
Author(s):  
Marta Soler ◽  
Marta González-Bártulos ◽  
David Soriano-Castell ◽  
Xavi Ribas ◽  
Miquel Costas ◽  
...  

BP16is a non-toxic cell-penetrating peptide with high cellular uptakein vitro. This peptide is an efficient vector for the delivery of therapeutic agents into cells, as has been shown for the anticancer drug chlorambucil.


Nanoscale ◽  
2021 ◽  
Author(s):  
Sanjay Pal ◽  
Vijay Soni ◽  
Sandeep Kumar ◽  
Somesh K Jha ◽  
Nihal Medatwal ◽  
...  

We present a non-immunogenic, injectable, low molecular weight, amphiphilic hydrogel-based drug delivery system (TB-Gel) that can entrap a cocktail of four front-line antitubercular drugs isoniazid, rifampicin, pyrazinamide, and ethambutol. We...


2009 ◽  
Vol 379 (1) ◽  
pp. 131-138 ◽  
Author(s):  
Ning Li ◽  
Chunyang Zhuang ◽  
Mi Wang ◽  
Xiyang Sun ◽  
Shufang Nie ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document