ควอนตัมดอทที่ทำให้เสถียรด้วยพอลิเมอร์คอนจูเกตกับแมนโนสสำหรับการตรวจติดตามทางชีวภาพ

This research aims to prepare water-soluble and biocompatible quantum dots (QDs) that are capable of targeting abnormal cells having enriched mannose receptors. 2’- Aminoethyl-α-D-mannopyranoside was first synthesized from 1,2,3,4,6-penta-O-acetyl-Dmannopyranose via 3-step reaction; glycosylation, d...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: ณัฐณิชา เลิศอมรมีสุข
مؤلفون آخرون: วรวีร์ โฮเว่น
التنسيق: Senior Project
اللغة:Thai
منشور في: จุฬาลงกรณ์มหาวิทยาลัย 2015
الموضوعات:
الوصول للمادة أونلاين:https://digiverse.chula.ac.th/Info/item/dc:9944
الوسوم: إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
الوصف
الملخص:This research aims to prepare water-soluble and biocompatible quantum dots (QDs) that are capable of targeting abnormal cells having enriched mannose receptors. 2’- Aminoethyl-α-D-mannopyranoside was first synthesized from 1,2,3,4,6-penta-O-acetyl-Dmannopyranose via 3-step reaction; glycosylation, deprotection, and hydrogenation. The synthesized mannose derivative was then conjugated with poly(methacrylic acid)-co-(2- methacryloyloxyethyl phosphorylcholine) (PMAMPC) having targeted degree of polymerization of 100 and comonomer ratio (MA:MPC) of 60:40 that was synthesized by RAFT polymerization employing ethyl(dimethylaminopropyl) carbodiimide (EDC)/ N-hydroxysuccinimide (NHS) as coupling reagents and yielded PMAMPC-mannose. Chemical structures of all products obtained in each step of reactions were verified by ¹H NMR and FT-IR spectroscopy. Due to the low stability of the original QDs, we were unsuccessful in preparing QDs stabilized with PMAMPC-mannose via ligand exchange using ethanolamine as temporary soft-binding ligand.