Novel pH-responsive folate conjugated chitosan and thiolated carboxymethyl cellulose based nanoparticles: potential approach for site-specific targeting in colon cancer treatment

被引:0
作者
Hanan, Hanasul [1 ]
Pervaiz, Fahad [1 ]
Ijaz, Muhammad [2 ,3 ]
Arshad, Tahreem [1 ]
Saeed, Komal [4 ]
Javaid, Syeda Munazza [1 ]
Hussain, Pakeeza [1 ]
Majeed, Asma [5 ]
机构
[1] Islamia Univ Bahawalpur, Fac Pharm, Dept Pharmaceut, Bahawalpur 63100, Pakistan
[2] COMSATS Univ Islamabad, Dept Pharm, Lahore Campus, Lahore 54000, Pakistan
[3] Univ Coll Dublin, Sch Vet Med, Dublin, Ireland
[4] Islamia Univ Bahawalpur, Fac Chem & Biol Sci, Dept Bot, Bahawalpur 63100, Pakistan
[5] Hlth Serv Acad, Islamabad 44000, Pakistan
关键词
Carboxymethyl cellulose; Chitosan; Nanoparticles; DELIVERY; CYTOTOXICITY;
D O I
10.1016/j.ijbiomac.2025.143952
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The study objective was to develop folate decorated chitosan (CHT-FA) by the carbodiimide-mediated process to utilize the overexpressed folate receptors in the treatment of colon cancer. The substitution degree of FA to CHT was 1.4 %. FTIR and (HNMR)-N-1 ensured the successful conjugation of FA with CHT. Thermal analysis and XRD demonstrated the thermal stability and amorphous nature of CHT-FA after conjugation. Thiolation of carboxymethyl cellulose, having a 1612.35 mu mol/g thiol group, was achieved via oxidation followed by reductive amination. CHT-FA and thiolated carboxymethyl cellulose (CMC-SH) were utilized in the development of nanoparticles with eudragit S100 coating (EU-FU-CHT-FA/CMC-SH NPs) for targeted delivery to the colon. The fabricated NPs demonstrated a higher release pattern at 7.4 pH after <5 % release at 1.2 pH. CHT-FA/CMC-SH NPs showed enhanced mucoadhesion time by up to 237 min. Furthermore, compared to the FU solution, the MTT analysis showed that FU-CHT-FA/CMC-SH NPs had a more cytotoxic effect and increased cellular uptake in the Caco-2 cell line via the folate receptor-facilitated endocytosis process along with the consequence of thiolation which prevents closer of tight junction, resulting in enhanced cellular absorption. These findings support the potential of the developed NPs as a tumor-targeted therapeutic delivery.
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页数:15
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