Fabrication of poly(sarcosine), poly (ethylene glycol), and poly (lactic-co-glycolic acid) polymeric nanoparticles for cancer drug delivery was written by Bhattacharya, Sankha. And the article was included in Journal of Drug Delivery Science and Technology in 2021.Recommanded Product: 3-(Benzo[d]thiazol-2-yl)-7-(diethylamino)-2H-chromen-2-one The following contents are mentioned in the article:
The most significant advantage of polymeric nanoparticles is their systematic and target specific drug delivery properties. To understand such a phenomenon, in this experiment, an attempt was made to prepared Docetaxel loaded poly(sarcosine)(PSar) and poly (ethylene glycol) (PEG) coated poly (lactic-co-glycolic acid) [PLGA] nanoparticles; which could efficiently encapsulate any hydrophobic drugs. These types of PEG-coated nanoparticles have a marked tendency to avoid reticuloendothelial opsonization process by restricting macrophage uptake, which ultimately leads to enhance bioavailability and tissue distribution of drugs. In this research work categorically, the concentration of PSar and PEG was optimized. The cellular uptake efficiency percentage and IC50 value of Docetaxel and Docetaxel loaded different polymeric nanoparticles evaluated in various human cancer cell lines (U-87 MG, HeLa. C2BBe1, HCT-116, NCI-N87, NCI-H929-Luc-mCh-Puro). The PSar-PLGA-PEG-NPs have shown sustainable retention in blood with min. macrophage uptake as compared to PLGA-NPs and PSar-PLGA-NPs. Enhanced anti-tumor proliferative effects were shown in all the Docetaxel loaded nanoparticles as compared to native Docetaxel drug, which may be because of enhanced antiproliferative activities of nanoparticles. Thus, from the research outcomes, one thing is inevitable, i.e., the presence of PSar and PEG would increase the blood circulation time, and it can be used as a suitable carrier for any hydrophobic drug. This study involved multiple reactions and reactants, such as 3-(Benzo[d]thiazol-2-yl)-7-(diethylamino)-2H-chromen-2-one (cas: 38215-36-0Recommanded Product: 3-(Benzo[d]thiazol-2-yl)-7-(diethylamino)-2H-chromen-2-one).
3-(Benzo[d]thiazol-2-yl)-7-(diethylamino)-2H-chromen-2-one (cas: 38215-36-0) belongs to thiazole derivatives. The thiazole ring has been identified as a central feature of numerous natural products, perhaps the most famous example of which is epothilone.Various laboratory methods exist for the organic synthesis of thiazoles. For example, 2,4-dimethylthiazole is synthesized from thioacetamide and chloroacetone.Recommanded Product: 3-(Benzo[d]thiazol-2-yl)-7-(diethylamino)-2H-chromen-2-one
Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica