Literature DB >> 26354801

Novel Nanostructured Solid Materials for Modulating Oral Drug Delivery from Solid-State Lipid-Based Drug Delivery Systems.

Tahnee J Dening1, Shasha Rao1, Nicky Thomas1, Clive A Prestidge2.   

Abstract

Lipid-based drug delivery systems (LBDDS) have gained significant attention in recent times, owing to their ability to overcome the challenges limiting the oral delivery of poorly water-soluble drugs. Despite the successful commercialization of several LBDDS products over the years, a large discrepancy exists between the number of poorly water-soluble drugs displaying suboptimal in vivo performances and the application of LBDDS to mitigate their various delivery challenges. Conventional LBDDS, including lipid solutions and suspensions, emulsions, and self-emulsifying formulations, suffer from various drawbacks limiting their widespread use and commercialization. Accordingly, solid-state LBDDS, fabricated by adsorbing LBDDS onto a chemically inert solid carrier material, have attracted substantial interest as a viable means of stabilizing LBDDS whilst eliminating some of the various limitations. This review describes the impact of solid carrier choice on LBDDS performance and highlights the importance of appropriate solid carrier material selection when designing hybrid solid-state LBDDS. Specifically, emphasis is placed on discussing the ability of the specific solid carrier to modulate drug release, control lipase action and lipid digestion, and enhance biopharmaceutical performance above the original liquid-state LBDDS. To encourage the interested reader to consider their solid carrier choice on a higher level, various novel materials with the potential for future use as solid carriers for LBDDS are described. This review is highly significant in guiding future research directions in the solid-state LBDDS field and fostering the translation of these delivery systems to the pharmaceutical marketplace.

Entities:  

Keywords:  lipid-based drug delivery systems; oral bioavailability; poorly water-soluble drugs; solid carriers; solid dosage forms

Mesh:

Substances:

Year:  2015        PMID: 26354801      PMCID: PMC4706287          DOI: 10.1208/s12248-015-9824-7

Source DB:  PubMed          Journal:  AAPS J        ISSN: 1550-7416            Impact factor:   4.009


  82 in total

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Journal:  Eur J Pharm Sci       Date:  2011-10-28       Impact factor: 4.384

Review 2.  Oral lipid-based formulations.

Authors:  David J Hauss
Journal:  Adv Drug Deliv Rev       Date:  2007-05-26       Impact factor: 15.470

3.  Internally structured pickering emulsions stabilized by clay mineral particles.

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Journal:  J Colloid Interface Sci       Date:  2009-02-24       Impact factor: 8.128

Review 4.  Transforming lipid-based oral drug delivery systems into solid dosage forms: an overview of solid carriers, physicochemical properties, and biopharmaceutical performance.

Authors:  Angel Tan; Shasha Rao; Clive A Prestidge
Journal:  Pharm Res       Date:  2013-06-18       Impact factor: 4.200

Review 5.  Mesoporous systems for poorly soluble drugs.

Authors:  Wujun Xu; Joakim Riikonen; Vesa-Pekka Lehto
Journal:  Int J Pharm       Date:  2012-09-08       Impact factor: 5.875

6.  The role of porous nanostructure in controlling lipase-mediated digestion of lipid loaded into silica particles.

Authors:  Paul Joyce; Angel Tan; Catherine P Whitby; Clive A Prestidge
Journal:  Langmuir       Date:  2014-03-04       Impact factor: 3.882

7.  Incomplete desorption of liquid excipients reduces the in vitro and in vivo performance of self-emulsifying drug delivery systems solidified by adsorption onto an inorganic mesoporous carrier.

Authors:  Michiel Van Speybroeck; Hywel D Williams; Tri-Hung Nguyen; Mette U Anby; Christopher J H Porter; Patrick Augustijns
Journal:  Mol Pharm       Date:  2012-08-07       Impact factor: 4.939

8.  Controlled release and antibacterial activity chlorhexidine acetate (CA) intercalated in montmorillonite.

Authors:  Na Meng; Ning-Lin Zhou; Shuang-Quan Zhang; Jian Shen
Journal:  Int J Pharm       Date:  2009-08-08       Impact factor: 5.875

9.  Inclusion of celecoxib into fibrous ordered mesoporous carbon for enhanced oral bioavailability and reduced gastric irritancy.

Authors:  Peng Zhao; Haitao Jiang; Tongying Jiang; Zhuangzhi Zhi; Chao Wu; Changshan Sun; Jinghai Zhang; Siling Wang
Journal:  Eur J Pharm Sci       Date:  2012-01-11       Impact factor: 4.384

10.  Nanocomposites of 2-arylpropionic acid drugs based on Mg-Al layered double hydroxide for dissolution enhancement.

Authors:  Mohamed R Berber; Keiji Minagawa; Masahiro Katoh; Takeshi Mori; Masami Tanaka
Journal:  Eur J Pharm Sci       Date:  2008-08-22       Impact factor: 4.384

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  6 in total

Review 1.  Current Status of Supersaturable Self-Emulsifying Drug Delivery Systems.

Authors:  Heejun Park; Eun-Sol Ha; Min-Soo Kim
Journal:  Pharmaceutics       Date:  2020-04-16       Impact factor: 6.321

Review 2.  Nano-fats for bugs: the benefits of lipid nanoparticles for antimicrobial therapy.

Authors:  Chelsea R Thorn; Nicky Thomas; Ben J Boyd; Clive A Prestidge
Journal:  Drug Deliv Transl Res       Date:  2021-03-05       Impact factor: 4.617

3.  In Vitro Performance and Chemical Stability of Lipid-Based Formulations Encapsulated in a Mesoporous Magnesium Carbonate Carrier.

Authors:  Caroline Alvebratt; Tahnee J Dening; Michelle Åhlén; Ocean Cheung; Maria Strømme; Adolf Gogoll; Clive A Prestidge; Christel A S Bergström
Journal:  Pharmaceutics       Date:  2020-05-06       Impact factor: 6.321

4.  Effects of Hydrophilic Carriers on Structural Transitions and In Vitro Properties of Solid Self-Microemulsifying Drug Delivery Systems.

Authors:  Tao Yi; Jifen Zhang
Journal:  Pharmaceutics       Date:  2019-06-08       Impact factor: 6.321

5.  Extended tacrolimus release via the combination of lipid-based solid dispersion and HPMC hydrogel matrix tablets.

Authors:  Hui Xu; Li Liu; Xuehui Li; Junyuan Ma; Rui Liu; Shaoning Wang
Journal:  Asian J Pharm Sci       Date:  2018-09-08       Impact factor: 6.598

6.  A novel solid self-nanoemulsifying drug delivery system (S-SNEDDS) for improved stability and oral bioavailability of an oily drug, 1-palmitoyl-2-linoleoyl-3-acetyl-rac-glycerol.

Authors:  Kyeong Soo Kim; Eun Su Yang; Dong Shik Kim; Dong Wuk Kim; Hye Hyun Yoo; Chul Soon Yong; Yu Seok Youn; Kyung Taek Oh; Jun-Pil Jee; Jong Oh Kim; Sung Giu Jin; Han Gon Choi
Journal:  Drug Deliv       Date:  2017-11       Impact factor: 6.419

  6 in total

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