FORMULASI NANOPARTIKEL RIBOSOME-INACTIVATING PROTEIN Mirabilis jalapa L. (RIP MJ) TERTARGET MENGGUNAKAN KITOSAN RANTAI PENDEK - PEKTIN TERKONJUGASI ANTIBODI ANTI-EPCAM DAN UJI SITOTOKSIK PADA SEL KANKER PAYUDARA
Ribosome Inactivating Proteins (RIPs) are protein from plants which depurinate ribosomal RNA. RIPs isolated from Mirabilis jalapa L. leaves showed higher cytotoxic effect on malignant cells (T47D and MCF7 cell line) more than on normal mononuclear cells. Chitosan nanoparticles have fr...
محفوظ في:
المؤلفون الرئيسيون: | , |
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التنسيق: | Theses and Dissertations NonPeerReviewed |
منشور في: |
[Yogyakarta] : Universitas Gadjah Mada
2014
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الموضوعات: | |
الوصول للمادة أونلاين: | https://repository.ugm.ac.id/133773/ http://etd.ugm.ac.id/index.php?mod=penelitian_detail&sub=PenelitianDetail&act=view&typ=html&buku_id=74590 |
الوسوم: |
إضافة وسم
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المؤسسة: | Universitas Gadjah Mada |
الملخص: | Ribosome Inactivating Proteins (RIPs) are protein from plants which
depurinate ribosomal RNA. RIPs isolated from Mirabilis jalapa L. leaves showed
higher cytotoxic effect on malignant cells (T47D and MCF7 cell line) more than
on normal mononuclear cells. Chitosan nanoparticles have frequently been used in
protein delivery applications. However studies regarding protein delivery using
chitosan nanoparticles modification with antibodi specifically targeting EpCAM
in tumor tissues are lacking. The aims of this study were to develop RIP MJ
entrapped into nanoparticles conjugated antiEpCAM, to characterized
nanoparticles of RIP MJ conjugated antiEpCAM, and to study cytotoxic effect on
T47D cell line.
RIPs loaded chitosan nanoparticles (RIPs CS-Pec NPs) were prepared
using low viscous chitosan and pectin as cross-linker with polyelectrolit complex
method, then conjugated with antiEpCAM antibodi by carbodiimide reaction.
AntiEpCAM conjugated RIPs CS-Pec nanoparticles was then characterized for its
entrapment efficiency, particles size, zeta potential, morphology by transmission
electron microscope (TEM) and cytotoxic assay on T47D and Vero cell line.
The optimal concentration of RIPs |
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