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발광성 실리콘 나노입자 약물전달체

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Author(s)
김세정
Issued Date
2023
Abstract
Chapter 1. Porous Silicon Nanoparticles as a Drug Delivery System

Today, Silicon nanoparticles with biocompatibility and biodegradability are promising candidates for drug DDS (Drug Delivery System). Porous silicon nanoparticles embedded in a PHEMA (polyhydrohexylmethacrylate) hydrogel matrix are prepared and used to measure the efficiency for controlled release drug delivery. Levofloxacin is a quinolone antibiotic medication and covalently bonded to a surface of porous silicon nanoparticles by condensation. The size of these particles is about a few decades nanometer. Since Levofloxacin has unique optical properties such as an electronic absorption and fluorescence, the release of levofloxacin has measured by fluorescence spectrometer. PL intensity analysis reveals that the porous silicon nanoparticles embedded in a hydrogel polymer matrix exhibit a great potential candidate for controlled release. The controlled drug-release profiles depend on the hydrolysis of Levofloxacin from the surface of porous silicon nanoparticles.


Chapter 2. One-pot Synthesis of Water-Soluble SiliconQuantum Dots

Silicon quantum dots (Si QDs) are promising candidate nano-materials for biological applications due to biocompatibility and biodegradability. Also, Si QDs have unique optical properties. New water-soluble silicon quantum dots (Si QDs) with photoluminescence (PL) in the visible region are simply prepared in one-pot synthesis at room temperature for biomedical applications. Methoxy-derivatized Si QDs, Hydroxide-derivatized Si QDs, Ethylene glycol-derivatized Si QDs, HEA-derivatized Si QDs are water-soluble and their PL characteristics were investigated by PL spectroscopy. The water-soluble Methoxy-derivatized Si QDs, Hydroxide-derivatized Si QDs, Ethylene glycol-derivatized Si QDs, HEA-derivatized Si QDs emit the PL at 420 nm, 408nm, with a full-width at half maximum height (FWHM) of 90 nm, 84nm, 95nm, 83nm in Methanol soultion. Absolute quantum yields were measured in Methanol soultion and were 8.4%, 6.1%, 10.4%, 5%. The integrated PL as a function of time for all water-soluble Si QDs indicates that the PL of water-soluble Si QDs are oxidized in a week. As a result, silicon quantum dots hope to contribute to biological applications.
Alternative Title
Luminescent Silicon Nanoparticles as a Drug Delivery System
Alternative Author(s)
Kim Se Jeong
Affiliation
조선대학교 일반대학원
Department
일반대학원 화학과
Advisor
손홍래
Awarded Date
2023-02
Table Of Contents
TABLE OF CONTENTS ⅰ
LIST OF SYMBOLS AND ABBREVIATIONS ⅳ
LIST OF TABLE ⅴ
LIST OF PICTURES ⅵ
LIST OF SCHEMES ⅶ
LIST OF FIGURES ⅸ

Chapter 1. 다공성 실리콘 나노입자를 이용한 약물전달시스템 1
Abstract 1

1. Introduction 2
1.1 약물 전달 시스템 (Drug Delivery system) 4
1.1.1 약물 4
1.1.2 약물 전달 시스템 (Drug Delivery System) 5
1.1.3 약물 투여 경로 및 목적 6
1.2 약물전달체 7
1.2.1 나노약물전달체 7
1.2.2 하이드로겔 8
1.2.3 다공성 실리콘 10
2. Experiment 12
2.1 Materials 12
2.2 Synthesis 13
2.2.1 다공성 실리콘 제작 13
2.2.2 다공성 실리콘 13
2.2.3 SiQD-Levo 제작 13
2.2.4 CL+Levo 제작 13
2.2.5 CL+ SiQD-Levo 제작 14
2.3 생체 외 방출실험 14
2.4 UV-vis spectroscopy 와 투과도 측정 15
2.5 PL spectroscopy 측정 15
3. Result and Discussion 16
3.1 FT-IR 분석 16
3.2 Photoluminescence properties 17
3.3 UV-Vis absorption / Hydrogel CL Transmittance properties 18
3.4 Release profile 20
4. Conclusion 21
5. References 22

Chapter 2. 수용성 실리콘 양자점 합성 25

Abstract 25

1. Introduction 26
1.1 양자점 28
1.1.1 양자점의 특성 28
1.1.2 실리콘 양자점 합성 30
1.1.3 Water soluble 실리콘 양자점 32
2. Experiment 34
2.1 Materials 34
2.2 Synthesis 35
2.2.1 Si QDs 제조 35
2.2.2 Si QD-OMe 제조 35
2.2.3 Si QD-OH 제조 36
2.2.4 Si QD-EG 제조 36
2.2.5 Si QD-HEA 제조 37
3. Results and Discussion 38
3.1 PL Spectroscopy 분석 38
3.2 QY 분석 47
3.3 FT-IR 분석 48
3.4 Life Time 측정 49
4. Conclusion 50
5. References 51
Degree
Master
Publisher
조선대학교 대학원
Citation
김세정. (2023). 발광성 실리콘 나노입자 약물전달체.
Type
Dissertation
URI
https://oak.chosun.ac.kr/handle/2020.oak/17647
http://chosun.dcollection.net/common/orgView/200000650913
Appears in Collections:
General Graduate School > 3. Theses(Master)
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