共遞送吉西他濱和多西他賽脂質(zhì)納米復(fù)合物的制備和藥效學(xué)研究
發(fā)布時(shí)間:2022-01-19 06:29
本論文主要從以下三個(gè)方面進(jìn)行研究:(1)共遞送吉西他濱和多西他賽脂質(zhì)納米復(fù)合物的制備、表征和體外評(píng)價(jià)GEM在DMSO溶劑環(huán)境中,在催化劑DCC和DMAP作用下,和HA發(fā)生酯化反應(yīng)脫水縮合,一步法合成了吉西他濱-透明質(zhì)酸前藥結(jié)合物HA-GEM,通過(guò)1H-NMR和FT-IR表征了化合物的化學(xué)結(jié)構(gòu),表明化合物合成成功,修飾率為11.83%,換算成質(zhì)量比為18.61%,載藥量較高。同時(shí),用DOTAP和膽固醇作為載體材料,采用薄膜水化法制備了載DTX陽(yáng)離子脂質(zhì)體,TEM照片顯示,制備的DTX-CLs外觀圓整,分散性較好,HPLC法測(cè)得載藥量6.15 ± 0.08%,包封率為 85.98 ± 1.59%,粒徑為 149.9 ±4.6 nm,PDI 0.19 ±0.02,zeta 電勢(shì) 33.3± 4.6 mV,表面電勢(shì)較高,溶液穩(wěn)定性好。由于制備的HA-GEM前藥水溶性良好,在溶液中以聚陰離子大分子形式存在,通過(guò)將HA-GEM與DTX-CLs在水溶液中緩慢攪拌后孵育,二者通過(guò)電荷相互吸引作用制備了共載GEM和DTX的脂質(zhì)納米復(fù)合物Combo NCs。Combo NCs的粒徑增加到 186.7 ± ...
【文章來(lái)源】:山東大學(xué)山東省 211工程院校 985工程院校 教育部直屬院校
【文章頁(yè)數(shù)】:109 頁(yè)
【學(xué)位級(jí)別】:碩士
【部分圖文】:
圖1?GEM入胞激活和代謝失活的分子機(jī)制
圖2?Combo?NCs的抗腫瘤機(jī)制示意圖。Combo?NCs通過(guò)被MDA-MB-231??細(xì)胞上CD44受體靶向攝取進(jìn)入細(xì)胞內(nèi)溶酶體,然后在pH?5.0和HA酶共同作用??下釋放GEM和DTX,進(jìn)入細(xì)胞質(zhì)的DTX能夠調(diào)節(jié)CDA/dCK平衡,使dCK表??達(dá)上升,CDA表達(dá)下降,從而使GEM活性產(chǎn)物增多,增強(qiáng)GEM的藥效。??Figure?2?Schematic?diagram?of?the?antitumor?mechanism?of?Combo?NCs.??Combo?NCs?are?targeted?to?enter?into?intracellular?lysosomes?by?CD44?receptor?on??MDA-MB-231?cells,?and?then?release?GEM?and?DTX?under?the?combined?action?of??pH?5.0?and?HA?enzymes.?DTX?entering?the?cytoplasm?can?regulate?CDA/dCK??balance.?The?expression?of?dCK?was?increased,?and?the?expression?of?CDA?was??decreased.?As?a?result,?the?product?of?GEM?activity?was?increased,?thereby?enhancing??the?efficacy?of?GEM.??
圖1-2?Combo?NCs的制備方法和GEM藥物釋放示意圖。(I)通過(guò)化學(xué)反應(yīng)合成??HA-GEM;?(II)通過(guò)薄膜水化法制備DTX-CLs;?(III)通過(guò)DOTAP的季銨陽(yáng)離??子和HA的羧基陰離子靜電吸引作用制備了?Combo?NCs;?(IV)溶酶體中的酸性??環(huán)境引起HA-GEM酯鍵斷裂,釋放出游離GEM。??Figure?1-2?Schematic?illustration?of?preparation?methods?of?Combo?NCs?and?acid??cleavage?of?HA-GEM?to?release?gemcitabine.?(I)?Synthesis?of?HA-GEM?by?chemical??reaction.?(II)?Preparation?of?DTX-CLs?by?thin-film?hydration?method.?(Ill)??Fabrication?of?Combo?NCs?by?electrostatic?attraction?of?ammonium?cation?of?DOTAP??and?carboxyl?anion?of?HA.?(IV)?Acidic?milieu?in?lysosomes?triggers?cleavage?of?ester??bond?and?induces?release?of?GEM.??(見(jiàn)實(shí)驗(yàn)記錄0003368-p47)??2.?3?DTX-CLs和Combo?NCs的物理化學(xué)性質(zhì)表征??
本文編號(hào):3596379
【文章來(lái)源】:山東大學(xué)山東省 211工程院校 985工程院校 教育部直屬院校
【文章頁(yè)數(shù)】:109 頁(yè)
【學(xué)位級(jí)別】:碩士
【部分圖文】:
圖1?GEM入胞激活和代謝失活的分子機(jī)制
圖2?Combo?NCs的抗腫瘤機(jī)制示意圖。Combo?NCs通過(guò)被MDA-MB-231??細(xì)胞上CD44受體靶向攝取進(jìn)入細(xì)胞內(nèi)溶酶體,然后在pH?5.0和HA酶共同作用??下釋放GEM和DTX,進(jìn)入細(xì)胞質(zhì)的DTX能夠調(diào)節(jié)CDA/dCK平衡,使dCK表??達(dá)上升,CDA表達(dá)下降,從而使GEM活性產(chǎn)物增多,增強(qiáng)GEM的藥效。??Figure?2?Schematic?diagram?of?the?antitumor?mechanism?of?Combo?NCs.??Combo?NCs?are?targeted?to?enter?into?intracellular?lysosomes?by?CD44?receptor?on??MDA-MB-231?cells,?and?then?release?GEM?and?DTX?under?the?combined?action?of??pH?5.0?and?HA?enzymes.?DTX?entering?the?cytoplasm?can?regulate?CDA/dCK??balance.?The?expression?of?dCK?was?increased,?and?the?expression?of?CDA?was??decreased.?As?a?result,?the?product?of?GEM?activity?was?increased,?thereby?enhancing??the?efficacy?of?GEM.??
圖1-2?Combo?NCs的制備方法和GEM藥物釋放示意圖。(I)通過(guò)化學(xué)反應(yīng)合成??HA-GEM;?(II)通過(guò)薄膜水化法制備DTX-CLs;?(III)通過(guò)DOTAP的季銨陽(yáng)離??子和HA的羧基陰離子靜電吸引作用制備了?Combo?NCs;?(IV)溶酶體中的酸性??環(huán)境引起HA-GEM酯鍵斷裂,釋放出游離GEM。??Figure?1-2?Schematic?illustration?of?preparation?methods?of?Combo?NCs?and?acid??cleavage?of?HA-GEM?to?release?gemcitabine.?(I)?Synthesis?of?HA-GEM?by?chemical??reaction.?(II)?Preparation?of?DTX-CLs?by?thin-film?hydration?method.?(Ill)??Fabrication?of?Combo?NCs?by?electrostatic?attraction?of?ammonium?cation?of?DOTAP??and?carboxyl?anion?of?HA.?(IV)?Acidic?milieu?in?lysosomes?triggers?cleavage?of?ester??bond?and?induces?release?of?GEM.??(見(jiàn)實(shí)驗(yàn)記錄0003368-p47)??2.?3?DTX-CLs和Combo?NCs的物理化學(xué)性質(zhì)表征??
本文編號(hào):3596379
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