(Q37910262)

25 August 2017

1 reference

title

Oral formulation strategies to improve solubility of poorly water-soluble drugs (English)

1 reference

25 August 2017

Abhishek Singh

1

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25 August 2017

Zelalem Ayenew Worku

series ordinal

2

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25 August 2017

Guy Van den Mooter

series ordinal

3

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25 August 2017

language of work or name

English

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publication date

3 August 2011

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Expert Opinion on Drug Delivery

25 August 2017

published in

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25 August 2017

volume

8

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25 August 2017

issue

10

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25 August 2017

page(s)

1361-1378

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Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system.

25 August 2017

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1 reference

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Challenges and solutions for the delivery of biotech drugs--a review of drug nanocrystal technology and lipid nanoparticles

21 January 2018

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Improving drug solubility for oral delivery using solid dispersions

21 January 2018

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Pharmaceutical Applications of Solid Dispersion Systems

21 January 2018

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Review: physical chemistry of solid dispersions

21 January 2018

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Spectroscopic characterization of interactions between PVP and indomethacin in amorphous molecular dispersions.

21 January 2018

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The mechanisms of drug release from solid dispersions in water-soluble polymers

21 January 2018

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https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs

21 January 2018

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https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Solubility-excipient classification gradient maps.

21 January 2018

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https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Cyclodextrins in drug delivery.

21 January 2018

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Elimination of bitter, disgusting tastes of drugs and foods by cyclodextrins

21 January 2018

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Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization

21 January 2018

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Cyclodextrins as pharmaceutical solubilizers.

21 January 2018

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Improvement of some pharmaceutical properties of DY-9760e by sulfobutyl ether beta-cyclodextrin

21 January 2018

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The equilibrium constant of beta-cyclodextrin-phenolphtalein complex; influence of temperature and tetrahydrofuran addition.

21 January 2018

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Solubilization of tropicamide by hydroxypropyl-beta-cyclodextrin and water-soluble polymers: in vitro/in vivo studies

21 January 2018

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The utility of cyclodextrins for enhancing oral bioavailability

21 January 2018

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https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Medicinal applications of cyclodextrins

21 January 2018

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https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Cyclodextrins and their pharmaceutical applications.

21 January 2018

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https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Mechanisms of drug release from cyclodextrin complexes

21 January 2018

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Cyclodextrins as solubilizers: formation of complex aggregates

21 January 2018

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Practical considerations in development of solid dosage forms that contain cyclodextrin

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Oral lipid-based formulations

21 January 2018

1 reference

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Enhancing intestinal drug solubilisation using lipid-based delivery systems.

21 January 2018

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Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Formulation of lipid-based delivery systems for oral administration: materials, methods and strategies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Examination of the solubilization of drugs by bile salt micelles

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Approaches for the development of solid and semi-solid lipid-based formulations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Development of solid self-emulsifying drug delivery systems: preparation techniques and dosage forms

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Drug nanocrystals of poorly soluble drugs produced by high pressure homogenisation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Nanocrystals: industrially feasible multifunctional formulation technology for poorly soluble actives

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Inhibition of Sulfathiazole Crystal Growth by Polyvinylpyrrolidone

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Nanosizing for oral and parenteral drug delivery: a perspective on formulating poorly-water soluble compounds using wet media milling technology

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Top-down production of drug nanocrystals: nanosuspension stabilization, miniaturization and transformation into solid products.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Confinement and controlled release of bisphosphonates on ordered mesoporous silica-based materials.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Inclusion of ibuprofen in mesoporous templated silica: drug loading and release property.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Enhanced release of itraconazole from ordered mesoporous SBA-15 silica materials

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Functionalized SBA-15 materials as carriers for controlled drug delivery: influence of surface properties on matrix-drug interactions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Towards establishing structure-activity relationships for mesoporous silica in drug delivery applications

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Ordered mesoporous silica induces pH-independent supersaturation of the basic low solubility compound itraconazole resulting in enhanced transepithelial transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Physical state of poorly water soluble therapeutic molecules loaded into SBA-15 ordered mesoporous silica carriers: a case study with itraconazole and ibuprofen

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Novel crystalline solid dispersion of tranilast with high photostability and improved oral bioavailability

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Improved dissolution and pharmacokinetic behavior of cyclosporine A using high-energy amorphous solid dispersion approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Preparation of esomeprazole zinc solid dispersion and study on its pharmacokinetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Enhanced oral absorption of saquinavir with Methyl-Beta-Cyclodextrin-Preparation and in vitro and in vivo evaluation

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Improvement of oral bioavailability of flurbiprofen from flurbiprofen/beta-cyclodextrin inclusion complex by action of cinnarizine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Silica-lipid hybrid (SLH) microcapsules: a novel oral delivery system for poorly soluble drugs

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Enhanced oral bioavailability of dexibuprofen by a novel solid self-emulsifying drug delivery system (SEDDS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Formulation and in vitro and in vivo characterization of a phenytoin self-emulsifying drug delivery system (SEDDS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Solid self-emulsifying nitrendipine pellets: preparation and in vitro/in vivo evaluation

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Formulation design and photochemical studies on nanocrystal solid dispersion of curcumin with improved oral bioavailability

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

Preparation of stable nitrendipine nanosuspensions using the precipitation-ultrasonication method for enhancement of dissolution and oral bioavailability

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

A comparison of the solubility of danazol in human and simulated gastrointestinal fluids

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17425247.2011.606808

10.1517/17425247.2011.606808

21 January 2018

Identifiers

DOI

1 reference

25 August 2017

1 reference