scholarly journals Pectin Matrix as Oral Drug Delivery Vehicle for Colon Cancer Treatment

2010 ◽  
Vol 12 (1) ◽  
pp. 201-214 ◽  
Author(s):  
Tin Wui Wong ◽  
Gaia Colombo ◽  
Fabio Sonvico
2012 ◽  
Vol 129 (2) ◽  
pp. 714-720 ◽  
Author(s):  
Yichao Wang ◽  
Puwang Li ◽  
Zheng Peng ◽  
Feng Hua She ◽  
Ling Xue Kong

2015 ◽  
Vol 2015 ◽  
pp. 1-12 ◽  
Author(s):  
Abdalrahim F. A. Aisha ◽  
Amin Malik Shah Abdulmajid ◽  
Zhari Ismail ◽  
Salman A. Alrokayan ◽  
Khalid M. Abu-Salah

Xanthones are a group of oxygenated heterocyclic compounds with anticancer properties, but poor aqueous solubility and low oral bioavailability hinder their therapeutic application. This study sought to prepare a xanthones extract (81%  α-mangostin and 16%  γ-mangostin) in polymeric nanoparticles and to investigate its intracellular delivery and cytotoxicity toward colon cancer cells. The nanoparticles were prepared in Eudragit RL100 and Eudragit RS100 by the nanoprecipitation method at drug loading and entrapment efficiency of 20% and >95%, respectively. Freeze-drying of bulk nanoparticle solutions, using glucose or sucrose as cryoprotectants, allowed the collection of nanoparticles at >95% yield. Solubility of the xanthones extract was improved from 0.1 µg/mL to 1250 µg/mL. Transmission electron microscopy (TEM) and dynamic light scattering (DLS) of the freeze-dried final formulation showed the presence of cationic round nanoparticles, with particle size in the range of 32–130 nm. Scanning electron microscopy (SEM) showed the presence of nanospheres, and Fourier transform infrared (FTIR) spectroscopy indicated intermolecular interaction of xanthones with Eudragit polymers. Cellular uptake of nanoparticles was mediated via endocytosis and indicated intracellular delivery of xanthones associated with potent cytotoxicity (median inhibitory concentration26.3±0.22 µg/mL). Presented results suggest that cationic nanoparticles of xanthones may provide a novel oral drug delivery system for chemoprevention or treatment of intestinal and colon tumors.


Nanoscale ◽  
2018 ◽  
Vol 10 (6) ◽  
pp. 2866-2875 ◽  
Author(s):  
Yeying Wang ◽  
Xijian Liu ◽  
Guoying Deng ◽  
Jian Sun ◽  
Haikuan Yuan ◽  
...  

A tumor-targeted and multi-stimuli-responsive drug delivery vehicle (Se@SiO2–FA–CuS/DOX) was fabricated for combined PTT with chemotherapy of DOX and Se in cancer treatment.


Nanoscale ◽  
2019 ◽  
Vol 11 (34) ◽  
pp. 15958-15970 ◽  
Author(s):  
Qingling Song ◽  
Jiajia Jia ◽  
Xiuxiu Niu ◽  
Cuixia Zheng ◽  
Hongjuan Zhao ◽  
...  

Oral drug delivery systems (ODDSs) have attracted considerable attention in relation to orthotopic colon cancer therapy due to certain popular advantages.


Author(s):  
Kathpalia Harsha ◽  
Das Sukanya

Ion Exchange Resins (IER) are insoluble polymers having styrene divinylbenzene copolymer backbone that contain acidic or basic functional groups and have the ability to exchange counter ions with the surrounding aqueous solutions. From the past many years they have been widely used for purification and softening of water and in chromatographic columns, however recently their use in pharmaceutical industry has gained considerable importance. Due to the physical stability and inert nature of the resins, they can be used as a versatile vehicle to design several modified release dosage forms The ionizable drug is complexed with the resin owing to the property of ion exchange. This resin complex dissociatesin vivo to release the drug. Based on the dissociation strength of the drug from the drug resin complex, various release patterns can be achieved. Many formulation glitches can be circumvented using ion exchange resins such as bitter taste and deliquescence. These resins also aid in enhancing disintegrationand stability of formulation. This review focuses on different types of ion exchange resins, their preparation methods, chemistry, properties, incompatibilities and their application in various oral drug delivery systems as well as highlighting their use as therapeutic agents.


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