Biological properties and enzymatic degradation studies of clindamycin-loaded PLA/HAp microspheres prepared from crocodile bones

2017 ◽  
Vol 74 (12) ◽  
pp. 5181-5194
Author(s):  
Juntima Pradid ◽  
Wirunya Keawwatana ◽  
Upsorn Boonyang ◽  
Siree Tangbunsuk
Biomolecules ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 1003
Author(s):  
Zhuning Wu ◽  
Stefanie H. Korntner ◽  
Jos Olijve ◽  
Anne Maria Mullen ◽  
Dimitios I. Zeugolis

In the medical device sector, bloom index and residual endotoxins should be controlled, as they are crucial regulators of the device’s physicochemical and biological properties. It is also imperative to identify a suitable crosslinking method to increase mechanical integrity, without jeopardising cellular functions of gelatin-based devices. Herein, gelatin preparations with variable bloom index and endotoxin levels were used to fabricate non-crosslinked and polyethylene glycol succinimidyl glutarate crosslinked gelatin scaffolds, the physicochemical and biological properties of which were subsequently assessed. Gelatin preparations with low bloom index resulted in hydrogels with significantly (p < 0.05) lower compression stress, elastic modulus and resistance to enzymatic degradation, and significantly higher (p < 0.05) free amine content than gelatin preparations with high bloom index. Gelatin preparations with high endotoxin levels resulted in films that induced significantly (p < 0.05) higher macrophage clusters than gelatin preparations with low endotoxin level. Our data suggest that the bloom index modulates the physicochemical properties, and the endotoxin content regulates the biological response of gelatin biomaterials. Although polyethylene glycol succinimidyl glutarate crosslinking significantly (p < 0.05) increased compression stress, elastic modulus and resistance to enzymatic degradation, and significantly (p < 0.05) decreased free amine content, at the concentration used, it did not provide sufficient structural integrity to support cell culture. Therefore, the quest for the optimal gelatin crosslinker continues.


2001 ◽  
Vol 169 (1) ◽  
pp. 261-272 ◽  
Author(s):  
Gianluca Ciardelli ◽  
Alfonsina Rechichi ◽  
Piero Cerrai ◽  
Mario Tricoli ◽  
Niccoletta Barbani ◽  
...  

1994 ◽  
Vol 25 (2) ◽  
pp. 123-130 ◽  
Author(s):  
Yuichi Ohya ◽  
Kenji Ihara ◽  
Jun-ichi Murata ◽  
Tomoko Sugitou ◽  
Tatsuro Ouchi

2018 ◽  
Vol 155 ◽  
pp. 84-94 ◽  
Author(s):  
Carmen Valverde ◽  
Gerard Lligadas ◽  
Juan C. Ronda ◽  
Marina Galià ◽  
Virginia Cádiz

2021 ◽  
Vol 9 ◽  
Author(s):  
Agnieszka Staśkiewicz ◽  
Patrycja Ledwoń ◽  
Paolo Rovero ◽  
Anna Maria Papini ◽  
Rafal Latajka

Peptidomimetics play a fundamental role in drug design due to their preferential properties regarding natural peptides. In particular, compounds possessing nitrogen-containing heterocycles have been intensively studied in recent years. The triazolyl moiety incorporation decreases the molecule susceptibility to enzymatic degradation, reduction, hydrolysis, and oxidation. In fact, peptides containing triazole rings are a typical example of peptidomimetics. They have all the advantages over classic peptides. Both efficient synthetic methods and biological activity make these systems an interesting and promising object of research. Peptide triazole derivatives display a diversity of biological properties and can be obtained via numerous synthetic strategies. In this review, we have highlighted the importance of the triazole-modified peptidomimetics in the field of drug design. We present an overview on new achievements in triazolyl-containing peptidomimetics synthesis and their biological activity as inhibitors of enzymes or against cancer, viruses, bacteria, or fungi. The relevance of above-mentioned compounds was confirmed by their comparison with unmodified peptides.


Biomaterials ◽  
1997 ◽  
Vol 18 (21) ◽  
pp. 1411-1415 ◽  
Author(s):  
Giovanni Abatangelo ◽  
Rolando Barbucci ◽  
Paola Brun ◽  
Stefania Lamponi

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