2015
DOI: 10.1016/j.ajps.2014.12.006
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Overview of milling techniques for improving the solubility of poorly water-soluble drugs

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Cited by 354 publications
(230 citation statements)
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“…When reaching the critical speed the balls can achieve the highest point of the mill without detaching the wall. Above the critical velocity, it is possible to observe the cataract effect, as shown in Zone C of Figure 1 [12] .…”
Section: Introductionmentioning
confidence: 99%
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“…When reaching the critical speed the balls can achieve the highest point of the mill without detaching the wall. Above the critical velocity, it is possible to observe the cataract effect, as shown in Zone C of Figure 1 [12] .…”
Section: Introductionmentioning
confidence: 99%
“…The balls compose the milling elements and drive rollers help to rotate the milling chamber. Adapted from Loh et al [12] . 1000), to be used in determining the PSD.…”
Section: Chitosan Characterizationmentioning
confidence: 99%
“…Fine drug particulates are especially desired in formulations designed for parenteral, respiratory and transdermal use. Most drugs after crystallization have to be comminuted and this physical transformation is required to various extents, often to enhance processability or solubility especially for drugs with limited aqueous solubility [48]. Qing Yao et al [49] reported redispersion of the shell-forming nanoparticles to improve oral bioavailability of core-shell structured beads.…”
Section: Dispersion Of Nanoparticles By Beads Millmentioning
confidence: 99%
“…Also, nanocrystalline solid dispersion of coenzyme Q10 prepared with cold wet-milling system to enhance the dissolution and biopharmaceutical properties of CoQ10 [50]. The mechanisms by which milling enhances drug dissolution and solubility altering in the size, specific surface area and shape of the drug particles as well as milling induced amorphization and/or structural disordering of the drug crystal (mechano-chemical activation) [48].…”
Section: Dispersion Of Nanoparticles By Beads Millmentioning
confidence: 99%
“…Pharmaceutical researchers are constantly working on various approaches for the enhancement of drug solubility and dissolution of BCS Class II drugs which improve the therapeutic responses and overcome the toxic effects related to the higher dose. [1][2][3][4][5][6][7][8] For the enhancement of solubility and dissolution, pharmaceutical scientists have been used various approaches such as particle size reduction, i.e., micronization and nanoformulations, [9] salt formation, [10] prodrug and drug derivatization, [11] cosolvency, [12] use of surfactants, [13] cyclodextrin complexes, [14] change in crystal habit or cocrystals, [6] self-emulsifying drug delivery systems, [15] solid dispersions, [16] etc. Each technique has its own merits and demerits regarding solubility enhancement and selection of suitable one is mainly depends on the type of drug, polymers, therapeutic, and targeted delivery of drug which to be obtained.…”
Section: Introductionmentioning
confidence: 99%