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(Luận văn thạc sĩ) investigate of albumin porous holow fe3o4 nanoparticles for dual drug delivery
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(Luận văn thạc sĩ) investigate of albumin porous holow fe3o4 nanoparticles for dual drug delivery

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Mô tả chi tiết

THAI NGUYEN UNIVERSITY

UNIVERSITY OF AGRICULTURE AND FORESTRY

TRAN THI THUY HA

TOPIC TITTLE: INVESTIGATE OF ALBUMIN COATED POROUS

HOLLOW Fe3O4 NANOPARTICLES FOR DUAL DRUGS DELIVERY

BACHELOR THESIS

Study Mode: Full-time

Major: Environmental Science and Management

Faculty: International Training and Development Center

Batch: 2010-2015

Thai Nguyen, 15/01/2015

n

THAI NGUYEN UNIVERSITY

UNIVERSITY OF AGRICULTURE AND FORESTRY

TRAN THI THUY HA

TOPIC TITTLE: INVESTIGATE OF ALBUMIN COATED POROUS

HOLLOW Fe3O4 NANOPARTICLES FOR DUAL DRUGS DELIVERY

BACHELOR THESIS

Study Mode: Full-time

Major: Environmental Science and Management

Faculty: International Training and Development Center

Batch: 2010-2015

Thai Nguyen, 15/01/2015

n

ii

Thai Nguyen University of Agriculture and Forestry

Degree Program Bachelor of Environmental Science and Management

Student name Tran Thi Thuy Ha

Student ID DTN1053110065

Thesis Title Investigate of Albumin-Porous Holow Fe3O4 Nanoparticles for

Dual Drug Delivery

Supervisor(s) Prof. Huang Yu-Fen & Dr. Do Thi Ngoc Oanh

Abstract:

Dual-functional drug carrier has been a modern strategy in cancer treatment.

Photodynamic therapy (PDT) is a non-invasive treatment modality for selective

destruction of cancer malignant cells, which involves light irradiation, and a

photosensitizer for free radicals generation; hence archiving photocytotoxicity. On

the other hand, the use of a chemotherapeutic agent is most effective at killing cells

that are rapidly dividing. However, most of the photosensitizers and

chemotherapeutical agents lack of efficient bio-distribution and cellular uptake; for

instance the use of nanoparticles provides an ideal carrier of a photodynamic drug.

In the present work, a photosensitizer drug protoporphyrin IX (PpIX), and a

chemotherapeutic drug Doxorubicin (DOX), are encapsulated onto porous hollow

iron nanoparticles (PHNPs) via oil in water emulsion procedure using BSA as a

stabilizer, with the aim of a synergistic effect through a combination therapy.

Carriers were successfully characterized; sizes and charges were monitored via DLS

and Zeta Potential respectively. The intracellular uptake and localization of

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