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http://people.math.gatech.edu/~chomp/workshop/saylor.pdf
microstructural evolution (processing & release conditions) in controlled drug delivery systems. ¥ Complementary laboratory experiments are being conducted to elucidate these same relationships and to provide validation for the theory. ¥ A relatively simple microstructural metric based on computational homology has been proposed to link
https://www.sciencedirect.com/science/article/pii/0169409X9390025Y
Modulated release systems: In these systems, the drug release is controlled by the external stimuli such as pH, ionic strength, temperature, magnetism, ultrasound and electromagnetic radiation [116]. Hydrogels which would respond to these external stimuli can be used as controlled-release devices. X.Author: Nikolaos A. Peppas, Atul R. Khare
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3719420/
A release model for a complex device that consisted of spherical drug particles dispersed within a PLGA disc was created to describe a burst phase release from the surface of the device as well as a polymer degradation controlled release . The burst phase …Author: Daniel J. Hines, David L. Kaplan
http://www.thepharmajournal.com/vol1Issue10/Issue_dec_2012/3.1.pdf
the purpose behind controlling the drug delivery is to achieve more effective therapies while eliminating the potential for both under and overdosing. CONTROL RELEASE DOSAGE FORM The United States Pharmacopoeia (USP) defines1 the modified-release (MR) dosage form as “the one for which the drug release characteristics of
https://www.sciencedirect.com/topics/pharmacology-toxicology-and-pharmaceutical-science/controlled-drug-release
Polymers applied to controlled drug release are often referred to as treatment polymers. The main purpose of the application of polymers for drug delivery systems is in controlled drug release. In these usages, drugs are trapped or mixed in polymer matrices (Vilar et al., 2012).
https://www.semanticscholar.org/paper/Nano-and-Microparticles-as-Controlled-Drug-Delivery-M.N.V./1b6802cb8ea6963b7fe8d84ebabe221436467012
The research in this area is being carried out all over the world at a great pace. Research areas cover novel properties that have been developed increased efficiency of drug delivery, improved release profiles and drug targeting. The purpose of this review is to take a closer look at nano/microparticles as drug delivery devices.
https://www.sciencedirect.com/science/article/pii/S0378517318307245
Dec 01, 2018 · Controlled drug delivery systems have been utilized to enhance the therapeutic effects of many drugs by delivering drugs in a time-dependent and sustained manner. Here, with the aid of 3D printing technology, drug delivery devices were fabricated and tested using a model drug …Author: Anh-Vu Do, Kristan S. Worthington, Budd A. Tucker, Aliasger K. Salem
https://sites.ualberta.ca/~csps/JPPS3(2)/M.Kumar/particles.htm
Research areas cover novel properties that have been developed increased efficiency of drug delivery, improved release profiles and drug targeting. The purpose of this review is to take a closer look at nano/microparticles as drug delivery devices.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846103/
For matrix-type devices, drug release is mainly controlled by diffusion as detailed in Table 1, and the cumulative release is linear with respect to the square root of time (t 1/2). As for crosslinked PDMS network, the network density is described by the average molecular weight Mn (number average) of the crosslinked units [ 38 ].Author: Yao Fu, Weiyuan John Kao
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322773/
Mar 24, 2015 · Drug release from stimuli-responsive nanocarriers is controlled by internal or external stimuli such as temperature, pH, ionic strength, sound, and electric or magnetic fields (Abouelmagd et al.). As it is possible to localize the stimuli, these carriers have been explored for target-specific drug delivery.
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