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发文基金:国家自然科学基金全球变化研究国家重大科学研究计划国家科技重大专项更多>>
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5 条 记 录,以下是 1-9
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Oligoargi nine-modi tied biodegradable nanoparticles:A novel delivery carrier for oral administration of insulin
In recent years,cell-penetrating peptides(CPPs)have been proven to be a useful tool in improving the membrane ...
Xiao-li Liu,Wen-jian Zhang,Cao Xie,Gang Wei~*,Wei-yue Lu Key Laboratory of Smart Drug Delivery,Ministry of Education & PLA
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含眼膏基质的环孢素A脂质纳米分散体的表征与稳定性评价被引量:1
2014年
以中链脂肪酸甘油酯(MCT)为液态脂质,利用乳化溶剂挥发与高压均质相结合的方法制备了一种新颖的含眼膏基质的环孢素A(1)脂质纳米分散体(eye ointment-contained cyclosporine A lipid nanodispersion,1-EOCLN),用于治疗伴有炎症反应的重度干眼症。所得1-EOCLN平均粒径约90 nm,多分散系数小于0.2,ζ电位低于-25 mV,1的包封率高于99%。透射电镜照片显示,1-EOCLN外观形态圆整,眼膏基质均匀包裹在MCT形成的乳滴中,且主要分布于油水两相的界面。1-EOCLN的粒径与ζ电位对温度及光照敏感,4℃条件放置6个月较稳定。EOCLN保留了眼膏剂的润滑和修复泪膜功能,同时避免了眼膏剂顺应性差的不足,是一种具有临床应用前景的疏水性药物眼部递送载体。
张文见魏刚陆伟跃
关键词:环孢素A眼膏稳定性干眼症
寡肽转运载体PepT1的转运机制及其介导的药物吸收被引量:8
2013年
寡肽转运载体PepT1广泛分布于人和动物体内的多种器官和组织,其底物主要为蛋白水解后的二肽和三肽。本文综合文献,阐述PepT1的体内分布及其质子依赖型的转运机制,从空间结构的角度分析其对底物分子的选择性,介绍评价底物与PepT1二者间亲和活性的体内外模型及PepT1底物修饰策略在促进药物吸收方面的应用。
刘畅魏刚陆伟跃
关键词:转运机制
寡聚精氨酸促进胰岛素纳米粒肠道吸收被引量:4
2012年
探索一种穿膜肽寡聚精氨酸[poly(arginine)8,R8]修饰的可生物降解乳酸/羟基乙酸共聚物[poly(lactic-co-glycolic acid),PLGA]纳米粒作为胰岛素(insulin,INS)口服给药载体的可行性。采用复乳-溶剂挥发法制备包载胰岛素的PLGA纳米粒(INS-NP),R8经聚乙二醇桥联修饰于该纳米粒表面(R8-INS-NP)。对纳米粒进行理化性状表征及体外释放特性考察,并进行正常大鼠在体灌肠给药的药动学与药效学评价。所得纳米粒平均粒径为(179.0±5.2)nm,多分散系数为0.152±0.042,胰岛素包封率为(29.10±2.59)%,载药量为(5.05±0.50)%,体外释放呈先快后慢的两相模式。给药剂量为10 U.kg—1时,R8-INS-NP的降血糖效果显著优于同剂量的INS-NP,而且D-构型R8修饰的纳米粒(D-R8-INS-NP)吸收优于L-构型R8修饰的纳米粒(L-R8-INS-NP)。与皮下注射相比,INS-NP、L-R8-INS-NP和D-R8-INS-NP在体灌肠给药的相对生物利用度分别为0.52%、4.78%和8.39%,药理相对生物利用度分别为2.07%、3.90%和8.24%。纳米粒表面经R8修饰可促进其包载的胰岛素经肠道吸收,为实现多肽、蛋白类生物大分子口服给药提供了新思路。
刘晓丽张文见魏刚陆伟跃
关键词:胰岛素穿膜肽纳米粒肠道吸收
可活化细胞穿膜肽在肿瘤治疗领域的应用被引量:4
2014年
细胞穿膜肽(CPP)是具有穿透多种细胞膜功能的小分子多肽,能携带生物活性大分子物质进入细胞。由于CPP缺乏组织选择性和靶向性,限制了其在肿瘤治疗领域的应用。可活化细胞穿膜肽(ACPP)的出现给CPP的应用带来了曙光。本文重点介绍基于肿瘤微环境与正常组织之间的差异以及利用外源性物理刺激设计而成的ACPP在抗肿瘤药物靶向递送方面的应用。
张利魏刚陆伟跃
关键词:肿瘤
Intraocular gene delivery mediated by cell-penetrating peptide
Intraocular drug delivery is extraordinarily hampered by the defensive barriers of the eye,which makes the bio...
魏刚
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Inhibition of post-trabeculectomy fibrosis via topically instilled antisense oligonucleotide complexes co-loaded with fluorouracil被引量:4
2020年
Trabeculectomy is the mainstay of surgical glaucoma treatment,while the success rate was unsatistying due to postoperative scarring of the filtering blebs.Clinical countermeasures for scar prevention are intraoperative intervention or repeated subconjunctival injections.Herein,we designed a codelivery system capable of transporting fluorouracil and anti-TGF-β2 oligonucleotide to synergistically inhibit fibroblast proliferation via topical instillation.This co-delivery system was built based on a cationic dendrimer core(PAMAM),which encapsulated fluorouracil within hydrophobic cavity and condensed oligonucleotide with surface amino groups,and was further modified with hyaluronic acid and cell-penetrating peptide penetratin.The co-delivery system was self-assembled into nanoscale complexes with increased cellular uptake and enabled efficient inhibition on proliferation of fibroblast cells.In vivo studies on rabbit trabeculectomy models further confirmed the anti-fibrosis efficiency of the complexes,which prolonged survival time of filtering blebs and maintained their height and extent during wound healing process,exhibiting an equivalent effect on scar prevention compared to intraoperative infiltration with fluorouracil.Qualitative observation by immunohistochemistry staining and quantitative analysis by Western blotting both suggested that TGF-β2 expression was inhibited by the co-delivery complexes.Our study provided a potential approach promising to guarantee success rate of trabeculectomy and prolong survival time of filtering blebs.
Kuan JiangJunyi ChenLingyu TaiChang LiuXishan ChenGang WeiWeiyue LuWeisan Pan
关键词:TRABECULECTOMYPENETRATIN
Penetratin-modified oligonucleotidepolyplexes inhibit protein expression of intraocular tumor via topical instillation
Antisense oligonucleotides(ASOs) are gaining tremendous attention to oncotherapy for effective silencing of ta...
太玲钰Kuan JiangGang WeiWeisan PanWeiyue Lu
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多肽介导的非创伤性眼内基因递送(英文)
Intraocular drug delivery is extraordinarily hampered by the defensive barriers of the eye,which makes the bio...
魏刚
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