pH-responsive glucosamine anchored polydopamine coated mesoporous silica nanoparticles for delivery of Anderson-type polyoxomolybdate in breast cancer

被引:9
|
作者
Ramezani-Aliakbari, Maryam [1 ,2 ]
Varshosaz, Jaleh [1 ]
Mirian, Mina [1 ]
Khodarahmi, Ghadamali [1 ]
Rostami, Mahboubeh [1 ]
机构
[1] Isfahan Univ Med Sci, Sch Pharm & Pharmaceut Sci, Dept Pharmaceut, Esfahan, Iran
[2] Univ Tehran Med Sci, Sch Pharm, Dept Med Chem, Med Chem, Tehran, Iran
关键词
Anderson-type manganese polyoxomolybdate (POMo); barbara amorphous-15 mesoporous Silica (SBA-15); polydopamine (PDA); anticancer activity; nanoparticles (NPs); targeted drug delivery; DRUG-DELIVERY; SURFACE MODIFICATION; CELLULAR UPTAKE; POLYOXOMETALATE; HYBRID; ACID; ANTITUMOR; CONJUGATE; STABILITY; RETENTION;
D O I
10.1080/02652048.2022.2096139
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Aim This study aimed to develop novel pH-sensitive Glucosamine (Glu) targeted Polydopamine (PDA) coated mesoporous silica (SBA-15) nanoparticles (NPs) for selective delivery of anticancer Anderson-type manganese polyoxomolybdate (POMo) to breast cancer. Methods The POMo@SBA-PDA-Glu NPs were prepared via direct hydrothermal synthesis of SBA, POMo loading, in situ PDA post functionalization, and Glu anchoring; the chemical structures were fully studied by different characterisation methods. The anticancer activity was studied by MTT method and Annexin V-FITC apoptosis detection kit. Results The optimised NPs had a hydrodynamic size (HS) of 195 nm, a zeta potential (ZP) of -18.9 mV, a loading content percent (LC%) of 45%, and a pH-responsive release profile. The targeted NPs showed increased anticancer activity against breast cancer cell lines compared to the free POMo with the highest cellular uptake and apoptosis level in the MDA-MB-231 cells. Conclusions POMo@SBA-PDA-Glu NPs could be a promising anticancer candidate for further studies.
引用
收藏
页码:433 / 451
页数:19
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