Active Targeting Nanoparticle Self-Assembled from Cisplatin-Palbociclib Amphiphiles Ensures Optimal Drug Ratio for Combinatorial Chemotherapy was written by Xiang, Yucheng;Liu, Chendong;Chen, Liqiang;Li, Lian;Huang, Yuan. And the article was included in Advanced Therapeutics (Weinheim, Germany) in 2021.Recommanded Product: 3-(Benzo[d]thiazol-2-yl)-7-(diethylamino)-2H-chromen-2-one The following contents are mentioned in the article:
Triple neg. breast cancer (TNBC) not only exhibits aggressive progression and metastasis, but also responds to neither hormone therapy nor checkpoint blockade therapy. Thus, combinatorial chemotherapy is indispensable for TNBC treatment. However, due to the different pharmacokinetics of individual drugs and weak synergistic effects caused by random drug molar ratio in tumor, direct coadministration is far from satisfactory. Constructing a nanoscale drug delivery system with fixed drug molar ratios and maximum drug content is an urgent problem. Herein, an active targeting nanoparticle self-assembled from cisplatin-palbociclib amphiphiles with optimal drug ratio is reported. The combination of cisplatin and palbociclib at a molar ratio of 1:2 is found to have the best synergistic effect and is selected for follow-up studies. After conjugating two palbociclib mols. to one cisplatin mol., a fixed cisplatin/palbociclib (1:2) molar ratio is enabled and this amphiphilic conjugate can self-assemble into nanoparticles. A small amount of iRGD coupled 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-polyethylene glycol-2000 (DSPE-PEG-iRGD) that further stabilizes the nanoparticle is introduced to fabricate the desired nanoparticle (iRGD-PCN) and endow active tumor-targeting ability. On an orthotopic TNBC mouse model, iRGD-PCN efficiently accumulates in tumors and inhibits tumor growth. Addnl., the formation of lung metastasis nodes is also significantly suppressed. In general, the active targeting nanoparticles self-assembled from cisplatin-palbociclib amphiphiles provide options for combinatorial chemotherapy. 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. Thiazole is a five-membered, unsaturated, planar, π-excessive heteroaromatic containing one sulfur atom and one pyridine-type nitrogen atom at position 3 of the cyclic ring system. Various laboratory methods exist for the organic synthesis of thiazoles. Prominent is the Hantzsch thiazole synthesis is a reaction between haloketones and thioamides.Recommanded Product: 3-(Benzo[d]thiazol-2-yl)-7-(diethylamino)-2H-chromen-2-one
Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica