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Bioresorbable Electronic Patch (BEP) Enabled Active Control of Drug Delivery for Brain Tumor Therapy : 뇌종양 치료를 위한 능동적인 약물 전달 조절이 가능한 생분해성 전자 패치

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dc.contributor.advisor김대형-
dc.contributor.author서현선-
dc.date.accessioned2017-07-19T05:57:48Z-
dc.date.available2019-08-02-
dc.date.issued2016-08-
dc.identifier.other000000135952-
dc.identifier.urihttps://hdl.handle.net/10371/129419-
dc.description학위논문 (석사)-- 서울대학교 대학원 : 화학생물공학부, 2016. 8. 김대형.-
dc.description.abstractBrain tumor disease is one of the harshest human cancers to treat. The presence of blood-brain barrier which prevents penetration of drugs into brain and residual tumors after surgical resection make brain tumor disease still remain unsolvable. Recently, clinical efforts to overcome those limitation of existing treatment of brain tumor disease have reported. Especially, implantable drug delivery system using biodegradable polymer wafer has been clinically used. However, it has serious demerits that the drug delivery is uncontrollable and inefficient. Emerging of new drug delivery system with active controllability is highly demanding. Here, I demonstrate a bioresorbable electronic patch (BEP) enabled sustainable, controllable, and localized drug delivery for brain tumor therapy. A natural bioresorbable polymer, starch, is fabricated as a form of flexible patch for conformal contact with biological tissues. An anti-cancer drug named doxorubicin (DOX) is loaded in the starch patch. Functional group modification of starch enables sustainable release of drug by forming covalent bonding between starch and DOX. Bioresorbable magnesium (Mg) heater performs wireless RF heating resulting in thermal actuation of drug delivery by breaking the bonding. To prevent excessive heating, real-time temperature monitoring by wireless temperature sensor as a form of LC oscillator is achieved. Therapeutic effects of BEP is verified by in vivo demonstration include tumor recurrence analysis using MRI and survival study. Therefore, BEP enabled active control of drug delivery has a great potential for becoming a novel and efficient treatment of brain tumor disease.-
dc.description.tableofcontents1. Introduction 1
2. Bioresorbable starch patch 6
2.1. Fabrication of starch patch 6
2.2. Conformal adhesion of starch patch 9
2.3. Aldehyde functional group modification of starch 14
2.4. Adhesion test of modified starch patch 18
2.5. In vitro drug release profile of modified starch patch 20
3. Bioresorbable wireless electronics 25
3.1. Wireless RF heating of bioresorbable heater 25
3.2. Thermal actuation of DOX delivery by bioresorbable heater 31
3.3. Design and operation of bioresorbable temperature sensor 37
4. In vivo demonstration of bioresorbable electronic patch (BEP) 43
4.1. In vivo biocompatibility and bioresorbability of BEP 43
4.2. BEP treatment procedure of mouse subcutaneous human brain tumor model 48
4.3. Tumor recurrence analysis using MRI study 50
4.4. Survival study 54
5. Experimental Section 57
5.1. Materials 57
5.2. Aldehyde functional group modification of starch 57
5.3. Fabrication of starch patch 58
5.4. Flexibility test of starch patch depending on glycerol contents 58
5.5. Adhesion test of modified starch patch depending on aldehyde contents 59
5.6. Measurement of in vitro drug release profile of BEP 59
5.7. Fabrication of bioresorbable electronic heater / temperature sensor and transfer of the device to the starch patch 60
5.8. Doxorubicin assessment 61
5.9. Animal model study 61
5.10. Immunohistochemical staining 62
5.11. Magnetic resonance imaging (MRI) protocol 62
6. Conclusion 64
7. Reference 65
국문초록 68
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dc.formatapplication/pdf-
dc.format.extent1817212 bytes-
dc.format.mediumapplication/pdf-
dc.language.isoen-
dc.publisher서울대학교 대학원-
dc.subjectBioresorbable electronic patch-
dc.subject.ddc660-
dc.titleBioresorbable Electronic Patch (BEP) Enabled Active Control of Drug Delivery for Brain Tumor Therapy-
dc.title.alternative뇌종양 치료를 위한 능동적인 약물 전달 조절이 가능한 생분해성 전자 패치-
dc.typeThesis-
dc.contributor.AlternativeAuthorHyunseon Seo-
dc.description.degreeMaster-
dc.citation.pages74-
dc.contributor.affiliation공과대학 화학생물공학부-
dc.date.awarded2016-08-
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