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Development and application of modif...

Hill, Tanner Kinkade.

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Development and application of modified hylauronic acid derived nanoparticles for image guided surgery and drug delivery.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Development and application of modified hylauronic acid derived nanoparticles for image guided surgery and drug delivery./
作者:	Hill, Tanner Kinkade.
面頁冊數:	204 p.
附註:	Source: Dissertation Abstracts International, Volume: 76-11(E), Section: B.
Contained By:	Dissertation Abstracts International76-11B(E).
標題:	Pharmaceutical sciences. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3712422
ISBN:	9781321892406

Development and application of modified hylauronic acid derived nanoparticles for image guided surgery and drug delivery.
Hill, Tanner Kinkade.

Development and application of modified hylauronic acid derived nanoparticles for image guided surgery and drug delivery. - 204 p.

Source: Dissertation Abstracts International, Volume: 76-11(E), Section: B.

Thesis (Ph.D.)--Wake Forest University, 2015.

This item is not available from ProQuest Dissertations & Theses.

This work presents research using the natural carbohydrate glycosaminoglycan hyaluronic acid (HLA) as a hydrophilic polymer backbone for the synthesis of nanoscale polymeric micelles loaded with either the near infrared (NIR) fluorophore indocyanine green (ICG) for image guided surgery (IGS), or the fatty acid synthase (FASN) inhibitor Orlistat (ORL) for chemotherapy. Hydrophobic conjugates were synthesized and conjugated to HLA in order to drive self-assembly into nanoparticles (NPs) and load their respective payloads. Chemical composition was confirmed by mass spectrometry and NMR. NP self-assembly was confirmed by dynamic light scattering (DLS) and atomic force microscopy. Optical properties of ICG-loaded NPs, termed NanoICG, were examined and ICG loading was found to be dependent on the structure of the hydrophobic ligand. Fluorescence quenching was observed in aqueous solution, and fluorescence could be reactivated by dissolution in a H2O:DMSO mixture, or in PBS with bovine serum albumin (BSA). ICG release to BSA was observed in vitro. Nano-ICG was found to have negligible cytotoxicity at physiologically relevant concentrations. In vivo results in a xenograft mouse model demonstrated that NanoICG provided superior contrast between tumor and surrounding muscle tissue, and NanoICG successfully identified positive margins (PMs). ORL was successfully loaded into NPs, termed Nano-ORL, at a loading efficiency of approximately 98%. Hydrodynamic diameter was found to be dependent on ORL content. ORL extracted from Nano-ORL successfully inhibited FASN similarly to free ORL, and Nano-ORL inhibited lipid synthesis in cells at approximately the same level as free ORL. Nano-ORL was found to be more cytotoxic than free ORL, and it was found that pre-incubation of both Nano-ORL and free ORL for 24 hours resulted in significantly reduced cytotoxicity of free ORL, while Nano-ORL remained just as cytotoxic. Metabolic analysis showed that Nano-ORL has a similar, negative impact on cellular metabolism as free ORL. These results present novel contributions in the form of the comparison of hydrophobic ligand structure in the loading of ICG into NPs, and the improved tumor accumulation and contrast achieved in vivo. Additionally, these results present the first HLA-derived NP formulation of ORL for use as a FASN inhibitor chemotherapeutic, and show that Nano-ORL has equal or greater activity against cancer cell lines than free ORL.

ISBN: 9781321892406Subjects--Topical Terms:

3173021
Pharmaceutical sciences.

Development and application of modified hylauronic acid derived nanoparticles for image guided surgery and drug delivery.
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520 $a This work presents research using the natural carbohydrate glycosaminoglycan hyaluronic acid (HLA) as a hydrophilic polymer backbone for the synthesis of nanoscale polymeric micelles loaded with either the near infrared (NIR) fluorophore indocyanine green (ICG) for image guided surgery (IGS), or the fatty acid synthase (FASN) inhibitor Orlistat (ORL) for chemotherapy. Hydrophobic conjugates were synthesized and conjugated to HLA in order to drive self-assembly into nanoparticles (NPs) and load their respective payloads. Chemical composition was confirmed by mass spectrometry and NMR. NP self-assembly was confirmed by dynamic light scattering (DLS) and atomic force microscopy. Optical properties of ICG-loaded NPs, termed NanoICG, were examined and ICG loading was found to be dependent on the structure of the hydrophobic ligand. Fluorescence quenching was observed in aqueous solution, and fluorescence could be reactivated by dissolution in a H2O:DMSO mixture, or in PBS with bovine serum albumin (BSA). ICG release to BSA was observed in vitro. Nano-ICG was found to have negligible cytotoxicity at physiologically relevant concentrations. In vivo results in a xenograft mouse model demonstrated that NanoICG provided superior contrast between tumor and surrounding muscle tissue, and NanoICG successfully identified positive margins (PMs). ORL was successfully loaded into NPs, termed Nano-ORL, at a loading efficiency of approximately 98%. Hydrodynamic diameter was found to be dependent on ORL content. ORL extracted from Nano-ORL successfully inhibited FASN similarly to free ORL, and Nano-ORL inhibited lipid synthesis in cells at approximately the same level as free ORL. Nano-ORL was found to be more cytotoxic than free ORL, and it was found that pre-incubation of both Nano-ORL and free ORL for 24 hours resulted in significantly reduced cytotoxicity of free ORL, while Nano-ORL remained just as cytotoxic. Metabolic analysis showed that Nano-ORL has a similar, negative impact on cellular metabolism as free ORL. These results present novel contributions in the form of the comparison of hydrophobic ligand structure in the loading of ICG into NPs, and the improved tumor accumulation and contrast achieved in vivo. Additionally, these results present the first HLA-derived NP formulation of ORL for use as a FASN inhibitor chemotherapeutic, and show that Nano-ORL has equal or greater activity against cancer cell lines than free ORL.
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