Cytotoxic activity of acidic Ribosome-inactivating Proteins Mirabilis jalapa L. protein (IP MJ-C) nanoparticle formulated with low chain chitosan and low methylated pectin
Penulis/Author
Prof. Dr. apt. Sismindari, S.U. (2); Dr.rer.nat. Ronny Martien, M.Si. (3); Dr. Hilda Ismail, M.Si., Apt. (4); Dr. Agustinus Yuswanto, SU., Apt. (5)
Tanggal/Date
19 2017
Kata Kunci/Keyword
Abstrak/Abstract
Mirabilis jalapa leaves were revealed to contain more than one ribosome inactivating proteins (RIP): RIP MJ-30 (basic RIP MJ) and MJ-C (acidic RIP MJ) [1-2]. Both of the RIPs have the ability to cleave supercoiled DNA into nick circular and linear form. It was found that RIP MJ-C has a more cytotoxic effect than RIP MJ-30 [3]. Therefore, RIP MJ-C could be developed as a potential anticancer agent. The challenge of RIP MJ-C delivery is that it could be easily
degraded in the body and have potential difficulties in entering
targeted cells [4-5]. Nanoparticle formulation would be one of the
way to resolve these problems and improving protein activity
against cancer cells [6-7]. Nanoparticles could be defined as colloidal
particles with a size range of 10-1000 nm, forming a polymer wall or
as a whole is formed as a matrix formed by polymers [8].
Nanoparticles formulated using biopolymers such as chitosan has
been known to increase the effectivity of various anticancer drug
delivery [9]. Previous work indicated that nanoparticle designed
from low chain chitosan and high methylated pectin showed good
potential for improving unpurified RIP MJ activity against MCF7
breast cancer cell-line [10]. A similar result was also found from
unpurified RIP MJ nanoparticle formulated by medium chain
chitosan and high methylated as well as low chained chitosan and
alginate [11, 12]. Therefore, in this research, we explored the use of
another formula using low chain chitosan and low methylated pectin
as a delivery system for RIP MJ-C, a purified acidic RIP MJ protein.
One of the ways to improve the selectivity and effectiveness of
nanoparticle delivery system is by conjugating nanoparticles to
molecules that could specifically reach target cancer cells. This was
exemplified by conjugation of ribonucleic acid (RNA) A10 to poly
(D,L-lactic-co-glycolic acid)-b-poly(ethylene glycol) (PLGA-b-PEG)
nanoparticles containing cisplatin and dual-aptamer based
doxorubicin delivery system for prostate cancer targeted therapy
[13-15]. Other molecule target that might be used is epithelial cell adhesion molecule (EpCAM), a monomer membrane glycoprotein
found within the normal human epithelium. EpCAM could serve as a
molecular marker between cancer cells and normal cells since it was
found to be over expressed on breast cancer cells [16]. By
conjugating nanoparticle to an anti-EpCAM antibody, the toxic
proteins or drugs would presumably be carried specifically into
target cancer cells. Therefore, conjugation of anti-EpCAM antibody
conjugation to RIP MJ-C nanoparticles could help carry RIP MJ-C to
target cells without damaging the normal ones.
Rumpun Ilmu
Farmasetika dan Teknologi Farmasi
Bahasa Asli/Original Language
English
Level
Internasional
Status
Dokumen Karya
No
Judul
Tipe Dokumen
Aksi
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4_Cytotoxic Activity Of Acidic Ribosome Inactivating Proteins Mirabilis Jalapa L_ (Rip Mj-C) Nanoparticle Formulated With Low-Chain Chitosan And Low-Methylated Pectin.pdf
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Cytotoxic Activity Of Acidic Ribosome Inactivating Proteins Mirabilis Jalapa L_ (Rip Mj-C) Nanoparticle Formulated With Low-Chain Chitosan And Low-Methylated Pectin.pdf