相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Melt extrusion with poorly soluble drugs - An integrated review
Michael A. Repka et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2018)
Transformation of Biopharmaceutical Classification System Class I and III Drugs Into Ionic Liquids and Lipophilic Salts for Enhanced Developability Using Lipid Formulations
Hywel D. Williams et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2018)
Biorelevant Drug Solubility Enhancement Modeled by a Linear Solvation Energy Relationship
Andreas Niederquell et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2018)
The Application of Modeling and Prediction to the Formation and Stability of Amorphous Solid Dispersions
Kevin DeBoyace et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2018)
Lipophilic salts of poorly soluble compounds to enable high-dose lipidic SEDDS formulations in drug discovery
Michael Morgen et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2017)
Glass-forming ability of compounds in marketed amorphous drug products
Nicole Wyttenbach et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2017)
Oral hesperidin-Amorphization and improved dissolution properties by controlled loading onto porous silica
Qionghua Wei et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2017)
Mesoporous silica-based dosage forms improve bioavailability of poorly soluble drugs in pigs: case example fenofibrate
Joseph P. O'Shea et al.
JOURNAL OF PHARMACY AND PHARMACOLOGY (2017)
Triazole/Triazine-Functionalized Mesoporous Silica As a Hybrid Material Support for Palladium Nanocatalyst
Ali Saad et al.
LANGMUIR (2017)
Computational Models of the Gastrointestinal Environment. 1. The Effect of Digestion on the Phase Behavior of Intestinal Fluids
Woldeamanuel A. Birru et al.
MOLECULAR PHARMACEUTICS (2017)
The Need for Restructuring the Disordered Science of Amorphous Drug Formulations
Khadijah Edueng et al.
PHARMACEUTICAL RESEARCH (2017)
Review and analysis of FDA approved drugs using lipid-based formulations
Ronak Savla et al.
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY (2017)
Stabilization and Amorphization of Lovastatin Using Different Types of Silica
Mai Khanfar et al.
AAPS PHARMSCITECH (2017)
Mesoporous silica formulation strategies for drug dissolution enhancement: a review
Carol A. McCarthy et al.
EXPERT OPINION ON DRUG DELIVERY (2016)
Mesoporous silica-based dosage forms improve release characteristics of poorly soluble drugs: case example fenofibrate
Jennifer B. Dressman et al.
JOURNAL OF PHARMACY AND PHARMACOLOGY (2016)
Theoretical Considerations of the Prigogine-Defay Ratio with Regard to the Glass-Forming Ability of Drugs from Undercooled Melts
Nicole Wyttenbach et al.
MOLECULAR PHARMACEUTICS (2016)
Lipophilic Prodrugs of SN38: Synthesis and in Vitro Characterization toward Oral Chemotherapy
Vaskor Bala et al.
MOLECULAR PHARMACEUTICS (2016)
Tools for Early Prediction of Drug Loading in Lipid-Based Formulations
Linda C. Alskar et al.
MOLECULAR PHARMACEUTICS (2016)
Computational prediction of formulation strategies for beyond-rule-of-5 compounds
Christel A. S. Bergstrom et al.
ADVANCED DRUG DELIVERY REVIEWS (2016)
50 years of oral lipid-based formulations: Provenance, progress and future perspectives
Orlagh M. Feeney et al.
ADVANCED DRUG DELIVERY REVIEWS (2016)
Cyclodextrins in pharmaceutical formulations II: solubilization, binding constant, and complexation efficiency
Sunil S. Jambhekar et al.
DRUG DISCOVERY TODAY (2016)
Ordered mesoporous silica to enhance the bioavailability of poorly water-soluble drugs: Proof of concept in man
Katarina Bukara et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2016)
Rapid determination of drug solubilization versus supersaturation in natural and digested lipids
Nicolas Gautschi et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2016)
Enhanced oral delivery of celecoxib via the development of a supersaturable amorphous formulation utilising mesoporous silica and co-loaded HPMCAS
A. -L. Laine et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2016)
Initial Drug Dissolution from Amorphous Solid Dispersions Controlled by Polymer Dissolution and Drug-Polymer Interaction
Yuejie Chen et al.
PHARMACEUTICAL RESEARCH (2016)
Classification of solid dispersions: correlation to (i) stability and solubility (ii) preparation and characterization techniques
Fan Meng et al.
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY (2015)
Loading amorphous Asarone in mesoporous silica SBA-15 through supercritical carbon dioxide technology to enhance dissolution and bioavailability
Zhengzan Zhang et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2015)
Physical stability of drugs after storage above and below the glass transition temperature: Relationship to glass-forming ability
Amjad Alhalaweh et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2015)
Transformation of Poorly Water-Soluble Drugs into Lipophilic Ionic Liquids Enhances Oral Drug Exposure from Lipid Based Formulations
Yasemin Sahbaz et al.
MOLECULAR PHARMACEUTICS (2015)
In Vitro Lipolysis Data Does Not Adequately Predict the In Vivo Performance of Lipid-Based Drug Delivery Systems Containing Fenofibrate
Nicky Thomas et al.
AAPS JOURNAL (2014)
Targeted delivery of a model immunomodulator to the lymphatic system: Comparison of alkyl ester versus triglyceride mimetic lipid prodrug strategies
Sifei Han et al.
JOURNAL OF CONTROLLED RELEASE (2014)
Solvent strategies for loading and release in mesoporous silica
Anna Hillerstrom et al.
COLLOID AND INTERFACE SCIENCE COMMUNICATIONS (2014)
Supersaturated Self-Nanoemulsifying Drug Delivery Systems (Super-SNEDDS) Enhance the Bioavailability of the Poorly Water-Soluble Drug Simvastatin in Dogs
Nicky Thomas et al.
AAPS JOURNAL (2013)
In silico prediction of the solubility advantage for amorphous drugs - Are there property-based rules for drug discovery and early pharmaceutical development?
Martin Kuentz et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2013)
Identifying the correlation between drug/stabilizer properties and critical quality attributes (CQAs) of nanosuspension formulation prepared by wet media milling technology
Maya George et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2013)
Early drug development predictions of glass-forming ability and physical stability of drugs
Denny Mahlin et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2013)
Current trends and future perspectives of solid dispersions containing poorly water-soluble drugs
Chau Le-Ngoc Vo et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2013)
Aqueous solubility: Simple predictive methods (in silico, in vitro and bio-relevant approaches)
David Elder et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2013)
Manufacturing of solid dispersions of poorly water soluble drugs by spray drying: Formulation and process considerations
Amrit Paudel et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2013)
Cyclodextrins
Sergey V. Kurkov et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2013)
Mesoporous systems for poorly soluble drugs
Wujun Xu et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2013)
Lipid-based formulations for oral administration of poorly water-soluble drugs
Huiling Mu et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2013)
Microstructure of an Immiscible Polymer Blend and Its Stabilization Effect on Amorphous Solid Dispersions
Ziyi Yang et al.
MOLECULAR PHARMACEUTICS (2013)
Computational Prediction of Drug Solubility in Lipid Based Formulation Excipients
Linda C. Persson et al.
PHARMACEUTICAL RESEARCH (2013)
Strategies to Address Low Drug Solubility in Discovery and Development
Hywel D. Williams et al.
PHARMACOLOGICAL REVIEWS (2013)
Development of novel microprecipitated bulk powder (MBP) technology for manufacturing stable amorphous formulations of poorly soluble drugs
Navnit Shah et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2012)
In vitro and in vivo performance of novel supersaturated self-nanoemulsifying drug delivery systems (super-SNEDDS)
N. Thomas et al.
JOURNAL OF CONTROLLED RELEASE (2012)
Cyclodextrins as functional excipients: Methods to enhance complexation efficiency
Thorsteinn Loftsson et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2012)
Nanosizing for oral and parenteral drug delivery: A perspective on formulating poorly-water soluble compounds using wet media milling technology
Elaine Merisko-Liversidge et al.
ADVANCED DRUG DELIVERY REVIEWS (2011)
Nanonization strategies for poorly water-soluble drugs
Huabing Chen et al.
DRUG DISCOVERY TODAY (2011)
Structure-based in silico model profiles the binding constant of poorly soluble drugs with β-cyclodextrin
Haiyan Li et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2011)
Comparison of mesoporous silicon and non-ordered mesoporous silica materials as drug carriers for itraconazole
Paivi Kinnari et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2011)
Higuchi equation: Derivation, applications, use and misuse
Juergen Siepmann et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2011)
Delivery Formulations of Ordered and Nonordered Mesoporous Silica: Comparison of Three Drug Loading Methods
Tarja Limnell et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2011)
Spontaneous Crystalline-to-Amorphous Phase Transformation of Organic or Medicinal Compounds in the Presence of Porous Media, Part 1: Thermodynamics of Spontaneous Amorphization
Ken K. Qian et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2011)
Potential of ordered mesoporous silica for oral delivery of poorly soluble drugs
Monica Vialpando et al.
THERAPEUTIC DELIVERY (2011)
Utilization of agro-industrial and municipal waste materials as potential adsorbents for water treatment-A review
Amit Bhatnagar et al.
CHEMICAL ENGINEERING JOURNAL (2010)
Enhanced absorption of the poorly soluble drug fenofibrate by tuning its release rate from ordered mesoporous silica
Michiel Van Speybroeck et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2010)
Hydrophilic and hydrophobic amino acid copolymers for nano-comminution of poorly soluble drugs
M. K. Lee et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2010)
Cyclodextrin knowledgebase a web-based service managing CD-ligand complexation data
Eszter Hazai et al.
JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN (2010)
A Classification System to Assess the Crystallization Tendency of Organic Molecules from Undercooled Melts
Jared A. Baird et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2010)
Aging behavior of pharmaceutical formulations of itraconazole on SBA-15 ordered mesoporous silica carrier material
Randy Mellaerts et al.
MICROPOROUS AND MESOPOROUS MATERIALS (2010)
Oxidized Mesoporous Silicon Microparticles for Improved Oral Delivery of Poorly Soluble Drugs
Feng Wang et al.
MOLECULAR PHARMACEUTICS (2010)
Formulate-ability of ten compounds with different physicochemical profiles in SMEDDS
Thao Do Thi et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2009)
Prediction of solubility curves and melting properties of organic and pharmaceutical compounds
Fredrik L. Nordstrom et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2009)
Ordered mesoporous materials for drug delivery
Shaobin Wang
MICROPOROUS AND MESOPOROUS MATERIALS (2009)
Development of Improved Empirical Models for Estimating the Binding Constant of a beta-Cyclodextrin Inclusion Complex
Ravi Chari et al.
PHARMACEUTICAL RESEARCH (2009)
What determines drug solubility in lipid vehicles: Is it predictable?
Sagar S. Rane et al.
ADVANCED DRUG DELIVERY REVIEWS (2008)
Uniform Rattle-type Hollow Magnetic Mesoporous Spheres as Drug Delivery Carriers and their Sustained-Release Property
Wenru Zhao et al.
ADVANCED FUNCTIONAL MATERIALS (2008)
Top-down production of drug nanocrystals: Nanosuspension stabilization, miniaturization and transformation into solid products
Bernard Van Eerdenbrugh et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2008)
Characteristics of polymers enabling nano-comminution of water-insoluble drugs
J. Lee et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2008)
Determination of the activity of a molecular solute in saturated solution
Fredrik L. Nordstrom et al.
JOURNAL OF CHEMICAL THERMODYNAMICS (2008)
Molecular characteristics for solid-state limited solubility
Carola M. Wassvik et al.
JOURNAL OF MEDICINAL CHEMISTRY (2008)
Mesoporous silicon in drug delivery applications
Jarno Salonen et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2008)
Hydroxypropyl Methylcellulose Acetate Succinate-Based Spray-Dried Dispersions: An Overview
Dwayne T. Friesen et al.
MOLECULAR PHARMACEUTICS (2008)
Lipid-based Formulations for Danazol Containing a Digestible Surfactant, Labrafil M2125CS: In Vivo Bioavailability and Dynamic In Vitro Lipolysis
Anne Larsen et al.
PHARMACEUTICAL RESEARCH (2008)
Poorly soluble marketed drugs display solvation limited solubility
Christel A. S. Bergstroem et al.
JOURNAL OF MEDICINAL CHEMISTRY (2007)
The utility of cyclodextrins for enhancing oral bioavailability
Rebecca L. Carrier et al.
JOURNAL OF CONTROLLED RELEASE (2007)
Thermodynamics of tetracycline adsorption on silica
I. Turku et al.
ENVIRONMENTAL CHEMISTRY LETTERS (2007)
Combined use of crystalline salt forms and precipitation inhibitors to improve oral absorption of celecoxib from solid oral formulations
Hector R. Guzman et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2007)
Evaluation of mesoporous TCPSi, MCM-41, SBA-15, and TUD-1 materials as API carriers for oral drug delivery
T. Heikkila et al.
DRUG DELIVERY (2007)
The effect of different lipid based formulations on the oral absorption of lipophilic drugs:: The ability of in vitro lipolysis and consecutive ex vivo intestinal permeability data to predict in vivo bioavailability in rats
Arik Dahan et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2007)
Cyclodextrins as pharmaccutical solubilizers
Marcus E. Brewster et al.
ADVANCED DRUG DELIVERY REVIEWS (2007)
Preparation of glass solutions of three poorly water soluble drugs by spray drying, melt extrusion and ball milling
James E. Patterson et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2007)
Lipid formulation strategies for enhancing intestinal transport and absorption of P-glycoprotein (P-gp) substrate drugs:: In vitro/in vivo case studies
Panayiotis P. Constantinides et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2007)
Lipids and lipid-based formulations: optimizing the oral delivery of lipophilic drugs
Christopher J. H. Porter et al.
NATURE REVIEWS DRUG DISCOVERY (2007)
Solid-state NMR study of ibuprofen confined in MCM-41 material
Thierry Azais et al.
CHEMISTRY OF MATERIALS (2006)
Contribution of solid-state properties to the aqueous solubility of drugs
Carola M. Wassvik et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2006)
Formulation of poorly water-soluble drugs for oral administration: Physicochemical and physiological issues and the lipid formulation classification system
Colin W. Pouton
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2006)
Ordered mesoporous materials in the context of drug delivery systems and bone tissue engineering
Maria Vallet-Regi
CHEMISTRY-A EUROPEAN JOURNAL (2006)
Cyclodextrins in drug delivery: An updated review
R Challa et al.
AAPS PHARMSCITECH (2005)
Molecular properties related to the anomalous solubility of β-cyclodextrin
KJ Naidoo et al.
JOURNAL OF PHYSICAL CHEMISTRY B (2004)
Influence of pore size of MCM-41 matrices on drug delivery rate
P Horcajada et al.
MICROPOROUS AND MESOPOROUS MATERIALS (2004)
Nanosuspensions in drug delivery
BE Rabinow
NATURE REVIEWS DRUG DISCOVERY (2004)
Design and evaluation of cyclodextrin-based drug formulation
K Uekama
CHEMICAL & PHARMACEUTICAL BULLETIN (2004)
Cyclodextrin-based pharmaceutics: Past, present and future
ME Davis et al.
NATURE REVIEWS DRUG DISCOVERY (2004)
Silica particles:: A novel drug-delivery system
C Barbé et al.
ADVANCED MATERIALS (2004)
Physical stability and solubility advantage from amorphous celecoxib: The role of thermodynamic quantities and molecular mobility
Piyush Gupta et al.
MOLECULAR PHARMACEUTICS (2004)
Influences of material characteristics on ibuprofen drug loading and release profiles from ordered micro- and mesoporous silica matrices
J Andersson et al.
CHEMISTRY OF MATERIALS (2004)
Mechanism of cationic surfactant adsorption at the solid-aqueous interface
R Atkin et al.
ADVANCES IN COLLOID AND INTERFACE SCIENCE (2003)
Solid state radical recombination and charge transfer across the boundary between indomethacin and silica under mechanical stress
T Watanabe et al.
JOURNAL OF SOLID STATE CHEMISTRY (2002)
Molecular mobility of amorphous pharmaceuticals determined using differential scanning calorimetry
BC Hancock et al.
THERMOCHIMICA ACTA (2001)
Freezing behavior in porous glasses and MCM-41
M Sliwinska-Bartkowiak et al.
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS (2001)
Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems
CW Pouton
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2000)
Improving drug solubility for oral delivery using solid dispersions
C Leuner et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2000)
What is the true solubility advantage for amorphous pharmaceuticals?
BC Hancock et al.
PHARMACEUTICAL RESEARCH (2000)
分享论文
