Show simple item record

dc.identifier.urihttp://hdl.handle.net/11401/77057
dc.description.sponsorshipThis work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.en_US
dc.formatMonograph
dc.format.mediumElectronic Resourceen_US
dc.language.isoen_US
dc.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dc.typeThesis
dcterms.abstractCancer remains the second leading cause of death in the United States. Although tremendous efforts have been made in the area of cancer therapy, there is still no common cure for cancer. Paclitaxel, which is a microtubule stabilizer, is used as an antitumor agent against several cancers such as ovarian, lung, and breast cancer. However, paclitaxel shows poor antitumor activities against drug resistant cell lines, and may cause undesirable side effects. Over the past decades, significant achievements have been made in the development of new generation taxoids that exhibit increased cytotoxicity against resistant cancer cell lines. Additionally work has been done towards the development of tumor-targeting drug delivery systems (TTDDS) to selectively distinguish cancer cells from normal cells. Based on structure-activity relationship (SAR) studies on taxanes, second generation taxoid SB-T-1214 and third generation taxoids SB-T-121202, SB-T-121302, SB-T-121402, SB-T-121602, and SB-T-121702 were synthesized via the Ojima-Holton coupling reaction. The biological evaluation of these novel taxoids showed excellent IC50 values against certain drug sensitive and drug resistant cancer cell lines by MTT assays. Biotin receptors are overexpressed on the surface of some cancer cell lines to maintain rapid cancer cell growth. Dendrimers are well-defined three-dimensional macromolecules, which can be used to increase the payload of the drugs, targeting efficacy of the conjugate, and other biological and physiological properties. Based on this fact, two dendrimer-based multifunctional conjugates for tumor-targeting drug delivery were synthesized by employing biotin as targeting moiety and second generation taxoid SB-T-1214 as antitumor agent.
dcterms.available2017-09-20T16:51:48Z
dcterms.contributorDrueckhammer, Daleen_US
dcterms.contributorOjima, Iwaoen_US
dcterms.contributorNgai, Ming-Yu.en_US
dcterms.creatorSun, Yi
dcterms.dateAccepted2017-09-20T16:51:48Z
dcterms.dateSubmitted2017-09-20T16:51:48Z
dcterms.descriptionDepartment of Chemistryen_US
dcterms.extent174 pg.en_US
dcterms.formatMonograph
dcterms.formatApplication/PDFen_US
dcterms.identifierhttp://hdl.handle.net/11401/77057
dcterms.issued2016-12-01
dcterms.languageen_US
dcterms.provenanceMade available in DSpace on 2017-09-20T16:51:48Z (GMT). No. of bitstreams: 1 Sun_grad.sunysb_0771M_12762.pdf: 18884388 bytes, checksum: 2892ad12a137a980dd259cfe8420b381 (MD5) Previous issue date: 1en
dcterms.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dcterms.subjectChemistry -- Organic chemistry
dcterms.titleSynthesis of New Generation Taxoid Anticancer Agents and Dendrimer-Based Multifunctional Conjugates for Tumor-Targeting Drug Delivery
dcterms.typeThesis


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record