Deproteinized natural rubber latex/gelatinized starch blended films as drug delivery carrier

2017 ◽  
Vol 148 (7) ◽  
pp. 1223-1228 ◽  
Author(s):  
Rungtiwa Waiprib ◽  
Prapaporn Boonme ◽  
Wirach Taweepreda ◽  
Ekwipoo Kalkornsurapranee ◽  
Jirapornchai Suksaeree ◽  
...  
2015 ◽  
Vol 659 ◽  
pp. 45-49 ◽  
Author(s):  
Rungtiwa Waiprib ◽  
Wiwat Pichayakorn ◽  
Prapaporn Boonme ◽  
Wirach Taweepreda ◽  
Jirapornchai Suksaeree

This research aimed to study the compatibility and properties of deproteinized natural rubber latex (DNRL)/gelatinized starch blended films for use as transdermal patches. Various starches were previously gelatinized by heat treatment. Then, the DNRL/gelatinized starch blended films were prepared by simple mixing of DNRL with gelatinized starch and then drying at 50°C. The various parameters such as types (potato, sago, bean, corn, tapioca, rice and glutinous starches), amounts (5, 10, 15 and 20 part per hundred of rubber (phr)) and concentrations of gelatinized starch pastes (5, 10, 20 and 50%) were evaluated. It was found that all starch types could be blended as a homogeneous mixture with DNRL only in 5 phr. Bean starch also provided the good mixture in 10 and 15 phr. Rice and corn starches in the concentrations up to 20 phr could also be blended. Higher concentration of gelatinized starch pastes obtained the higher viscous liquids that were difficult to blend as a homogeneous mixture with DNRL, and provided inhomogeneous blended films. The dried films of all homogeneous DNRL/gelatinized starch mixtures were slightly yellowish transparent with good physical appearances. The tensile strength, swelling and erosion of these blended films increased when increasing amounts of gelatinized starch, but their elasticities were not different comparing to that of DNRL film itself. However, their strengths should be further improved by adding some plasticizers. Some drugs would be further loaded in these homogeneous film formulations for transdermal delivery.


2009 ◽  
Vol 12 (2) ◽  
pp. 253-256 ◽  
Author(s):  
Rondinelli Donizetti Herculano ◽  
Cecília Pereira Silva ◽  
Cibele Ereno ◽  
Sérgio Augusto Catanzaro Guimaraes ◽  
Angela Kinoshita ◽  
...  

2018 ◽  
Vol 42 (17) ◽  
pp. 14179-14187
Author(s):  
Janisha Jayadevan ◽  
G. Unnikrishnan

Novel blend membranes from physico-chemically modified deproteinized natural rubber latex for drug release applications.


Author(s):  
Roslim Ramli ◽  
Ai Bao Chai ◽  
Shamsul Kamaruddin ◽  
Jee Hou Ho ◽  
Fatimah Rubaizah Mohd. Rasdi ◽  
...  

2013 ◽  
Vol 844 ◽  
pp. 470-473
Author(s):  
Wiwat Pichayakorn ◽  
Prapaporn Boonme ◽  
Wirach Taweepreda

This study aimed to prepare the nicotine chewing gums for smoking cessation using deproteinized natural rubber latex (DNRL) as gum bases due to its highly flexible property. The formulations were produced by the conventional heat melting and kneading methods. The experimental design was used to obtain the optimum 3 gum base formulations. Each formulation composed of olive oil as a plasticizer; sodium carboxymethylcellulose as an adsorbent; xylitol, mannitol and saccharin sodium as sweeteners instead of sugar. Gum base 1 and gum base 2 had the same sweetener amount but gum base 2 had the lower plasticizer amount, while gum base 1 and gum base 3 had the same plasticizer amount but different sweetener amount. Nicotine was added into each 3 gum bases (NCT1-3). The results showed no significant difference of appearance and taste. Their physicochemical properties were as following: pH of 8.45, 8.46, 8.54, hardness of 39.80, 36.28, 33.14 Shore A, initial modulus of 0.090, 1.260, 0.065 MPa, %elongation of 286, 403, 489%, drug content of 63.62, 70.95, 72.70%, and drug release when 500 times for force clamping of 48.72, 45.72, 67.74%, respectively. After storage at room temperature for 1 month, NCT1 and NCT2 showed unchangeable appearance, but NCT3 showed the slightly liquefied film and much sticky due to hygroscopic property of its sweetener. However, all formulations showed the significant reduction of drug amount which should be further improved in their stability properties.


2013 ◽  
Vol 747 ◽  
pp. 91-94 ◽  
Author(s):  
Kamon Panrat ◽  
Prapaporn Boonme ◽  
Wirach Taweepreda ◽  
Wiwat Pichayakorn

Matrix is one of the most interesting drug delivery systems to control drug release in pharmaceutical dosage forms. Natural rubber latex (NRL) from Hevea brasiliensis consists of cis-1,4-polyisoprene as the major polymer. It presents interesting physical properties such as easy to manipulate, low cost, high mechanical resistance, and insoluble in water. The aim of this study was to use the NRL as binder in matrix tablets for controlling the release rate of drug. NRL, sodium carboxymethylcellulose, olive oil, Tween 80, and lactose were used as polymer, adsorbent, plasticizer, surfactant, and diluent, respectively. Propranolol hydrochloride was used as a model drug. Propranolol hydrochloride matrix tablets were prepared by conventional heat-melting method. The in vitro release of drug from matrix tablets was determined by UV-Vis method according to dissolution test under Propranolol Hydrochloride Tablets USP30-NF25 monograph. Morphology of propranolol hydrochloride matrix tablet before and after released study was observed by scanning electron microscopy (SEM). It was found that NRL matrix tablets could control the drug release up to 12 hours. The release profiles were best fitted with Higuchi model. NRL amounts affected the properties of the propranolol hydrochloride matrix tablets. Increasing the NRL quantity in the matrices provided the decrease of release rate of drug. SEM photographs showed the number, size, and distribution of pore in propranolol hydrochloride matrix tablets that depended on amount of NRL addition. These results confirmed that NRL was possible to use as binder for matrix tablets in oral drug delivery systems.


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