2013
DOI: 10.2174/22103031113039990005
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Solubility Enhancement of Modafinil by Complexation with β-cyclodextrin and Hydroxypropyl β-cyclodextrin: A Response Surface Modeling Approach

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Cited by 11 publications
(6 citation statements)
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“…The notable drawback of the hydrophobic drug in clinical practice is the poor solubility and low bioavailability after conventional administration (Mahapatra et al, 2013). Mesoporous materials are promising carriers for poorly soluble drugs.…”
Section: Mesoporous Carbon Nanomaterialsmentioning
confidence: 99%
“…The notable drawback of the hydrophobic drug in clinical practice is the poor solubility and low bioavailability after conventional administration (Mahapatra et al, 2013). Mesoporous materials are promising carriers for poorly soluble drugs.…”
Section: Mesoporous Carbon Nanomaterialsmentioning
confidence: 99%
“…Based primarily on the physicochemical properties of the active ingredients, a diverse strategy for active ingredient delivery has been proposed to increase the solubility and/or the rate of dissolution of such molecules. 6 These fascinating techniques include chemical modification, 7 cocrystals, 8 micro-/ nanonization, 3,5,6 polymorphic improvements, 9 lipid-based systems, 6,10 micellar solubilization in-cluding self-emulsifying drug delivery systems, 11 inclusion complexes, [12][13][14][15] amorphous solid dispersion/solution [16][17][18] etc. In addition, nanotechnology has provided solutions for improving the solubility and/or bioavailability of active ingredients.…”
Section: Introductionmentioning
confidence: 99%
“…The interaction between the host and guest molecules is solely van der Waals bonding. Inclusion complexation has been widely exploited by researchers worldwide for the improvement of drug solubility and subsequent improvement of drug bioavailability (Mahapatra et al, 2013; Mallick et al, 2007; Roy et al, 2020). The cyclodextrins are the wonderful host molecules often used in drug delivery science for the formation of inclusion complexes.…”
Section: Nanofiber For Delivery Of Poorly Soluble Drugsmentioning
confidence: 99%
“…Diverse drug delivery strategies have been suggested to improve the solubilization and/or the dissolution velocity of such molecules (Mallick et al, 2007; Mallick et al, 2008; Pattnaik & Pathak, 2017; Pattnaik, Swain, Rao, Talla, et al, 2015). These intriguing techniques encompass chemical modification (Mallick et al, 2007; Takahashi et al, 2020), co‐crystals (Nechipadappu et al, 2017; Teoh et al, 2020), micro/nanonization (Pattnaik, Swain, Manaswini, Divyavani, et al, 2015; Pattnaik, Swain, Rao, Varun, & Subudhi, 2015), polymorphic ameliorations (Liu et al, 2015), lipid‐based systems (Castro & Lindqvist, 2020; Rahman et al, 2019), micellar solubilization which includes self‐emulsifying drug delivery systems (Chou et al, 2020; Yang et al, 2019), inclusion complexes (Mahapatra et al, 2013), amorphous solid dispersion/solution (Guo et al, 2021; Smeets et al, 2018), etc. Nanotechnology has additionally contributed nicely to seeking solutions for improved solubility and/or bioavailability of drug substances (Panda et al, 2022; Pattnaik, Swain, Manaswini, Divyavani, et al, 2015; Pattnaik, Swain, Rao, Varun, & Subudhi, 2015).…”
Section: Introductionmentioning
confidence: 99%