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Relevant bibliographies by topics / Micromeritics

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Journal articles

Academic literature on the topic 'Micromeritics'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Micromeritics"

1

Himawan, A., N. J. N. Djide, M. Mudjahid, A. D. I. Lukita, A. Arjuna, and Aliyah. "Physicochemical and Micromeritics Properties of Ketoprofen-Tartaric Acid Binary System." Journal of Physics: Conference Series 1341 (October 2019): 072004. http://dx.doi.org/10.1088/1742-6596/1341/7/072004.

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2

Paramakrishnan, N., S. Jha, and K. Jayaram Kumar. "Effect of carboxymethylation on physicochemical, micromeritics and release characteristics of Kyllinga nemoralis starch." International Journal of Biological Macromolecules 92 (November 2016): 543–49. http://dx.doi.org/10.1016/j.ijbiomac.2016.07.039.

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3

Kedia, Kishori, and Sarika Wairkar. "Improved micromeritics, packing properties and compressibility of high dose drug, Cycloserine, by spherical crystallization." Powder Technology 344 (February 2019): 665–72. http://dx.doi.org/10.1016/j.powtec.2018.12.068.

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4

Ayon, Navid Jubaer, Ikramul Hasan, Md Shfiqul Islam, and Md Selim Reza. "Preparation and characterization of Gliclazide incorporated Cellulosic Microspheres: studies on drug release, compatibility and micromeritics." Dhaka University Journal of Pharmaceutical Sciences 13, no. 2 (2015): 149–66. http://dx.doi.org/10.3329/dujps.v13i2.21893.

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Polymeric microspheres of gliclazide were prepared to provide sustained release delivery of gliclazide to aid in continuous therapy with high margin of safety. Gliclazide was microencapsulated with different polymers namely HPMC K100LV, Ethocel (20 cps) and HPMC K100M by emulsion solvent evaporation technique using acetone as internal phase and liquid paraffin as external phase. Seventeen formulations were prepared using different drug loading and polymeric ratio of which nine formulations were prepared by a 32 full factorial design. Each formulation was evaluated for flow properties, particle

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5

Viswanathan, Chelakara L., Sushrut K. Kulkarni, and Dhanashri R. Kolwankar. "Spherical agglomeration of mefenamic acid and nabumetone to improve micromeritics and solubility: A technical note." AAPS PharmSciTech 7, no. 2 (2006): E122—E125. http://dx.doi.org/10.1208/pt070248.

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6

Ma, Cheng, Wenhao Wang, Zhengwei Huang, et al. "Effect of the cargo lipophilicity on powder micromeritics properties of drug-loaded solid lipid microparticles." Journal of Drug Delivery Science and Technology 51 (June 2019): 614–20. http://dx.doi.org/10.1016/j.jddst.2019.03.025.

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7

Pryszcz, Adrian, Barbora Grycová, Ivan Koutník, and Veronika Blahůšková. "Characterization of Tar Deposits, Extraction and Sorption Properties." GeoScience Engineering 62, no. 2 (2016): 1–4. http://dx.doi.org/10.1515/gse-2016-0010.

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Abstract The main goal of this paper was to characterize and find a useful solution for the decomposition of tar deposits. For the experimental part, tar deposits, formed by polymerization and condensation reactions, were chosen from a storage tank for tars. At first the initial analyses of tar deposits (elemental, thermogravimetric, and calorimetric analyses) were performed. After the characterization, the tar deposits were extracted in the Soxhlet extractor by acetone, toluene, and quinolone and activated with potassium hydroxide. As the final step of this work, the sorption characterization

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8

RILEY, C., S. ADEBAYO, A. WHEATLEY, and H. ASEMOTA. "The interplay between yam (Dioscorea sp.) starch botanical source, micromeritics and functionality in paracetamol granules for reconstitution." European Journal of Pharmaceutics and Biopharmaceutics 70, no. 1 (2008): 326–34. http://dx.doi.org/10.1016/j.ejpb.2008.03.001.

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9

Kaur, Harjeet, Baldeep Kumar, Amitava Chakrabarti, et al. "A New Therapeutic Approach for Brain Delivery of Epigallocatechin Gallate: Development and Characterization Studies." Current Drug Delivery 16, no. 1 (2018): 59–65. http://dx.doi.org/10.2174/1567201815666180926121104.

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Background: Blood-brain permeability is the primary concern when dealing with the biodistribution of drugs to the brain in neurological diseases. Objective: The purpose of the study is to develop the nanoformulation of Epigallocatechin gallate (EGCG) in order to improve its bioavailability and penetration into the brain. Methods: EGCG loaded Solid Lipid Nanoparticles (SLNs) have been developed using microemulsification method and pharmacological assessments were performed. Results: Surface morphology and micromeritics analysis showed the successful development of EGCG loaded solid lipid nanopa

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10

Rashad, Amira A., Sara Nageeb El-Helaly, Randa T. Abd El Rehim, and Omaima N. El-Gazayerly. "Core-in-cup/liquisol dual tackling effect on azelnidipine buccoadhesive tablet micromeritics, in vitro release, and mucoadhesive strength." Acta Pharmaceutica 69, no. 3 (2019): 381–98. http://dx.doi.org/10.2478/acph-2019-0022.

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Abstract Reduced bioavailability of azelnidipine is related to its poor aqueous solubility and extensive first-pass metabolism, which hinder its efficacy. These problems were addressed by implementing (1) a liquisol technique for promoting the dissolution rate in a controlled-release manner and (2) a core-in-cup bucco-adhesive drug delivery system as an alternative to the oral route. A 33 factorial design was used to study the effects of polymer type (sodium carboxymethyl cellulose (CMC Na), chitosan, or Carbomer P940) concentration (5, 10 or 15 %) and preparation technique (simple mix, liquis

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