Improved Vemurafenib Dissolution and Pharmacokinetics as an Amorphous Solid Dispersion Produced by KinetiSol® Processing.

Abstract:

:Vemurafenib is a poorly soluble, low permeability drug that has a demonstrated need for a solubility-enhanced formulation. However, conventional approaches for amorphous solid dispersion production are challenging due to the physiochemical properties of the compound. A suitable and novel method for creating an amorphous solid dispersion, known as solvent-controlled coprecipitation, was developed to make a material known as microprecipitated bulk powder (MBP). However, this approach has limitations in its processing and formulation space. In this study, it was hypothesized that vemurafenib can be processed by KinetiSol into the same amorphous formulation as MBP. The KinetiSol process utilizes high shear to rapidly process amorphous solid dispersions containing vemurafenib. Analysis of the material demonstrated that KinetiSol produced amorphous, single-phase material with acceptable chemical purity and stability. Values obtained were congruent to analysis conducted on the comparator material. However, the materials differed in particle morphology as the KinetiSol material was dense, smooth, and uniform while the MBP comparator was porous in structure and exhibited high surface area. The particles produced by KinetiSol had improved in-vitro dissolution and pharmacokinetic performance for vemurafenib compared to MBP due to slower drug nucleation and recrystallization which resulted in superior supersaturation maintenance during drug release. In the in-vivo rat pharmacokinetic study, both amorphous solid dispersions produced by KinetiSol exhibited mean AUC values at least two-fold that of MBP when dosed as a suspension. It was concluded that the KinetiSol process produced superior dosage forms containing vemurafenib with the potential for substantial reduction in patient pill burden.

journal_name

AAPS PharmSciTech

journal_title

AAPS PharmSciTech

authors

Ellenberger DJ,Miller DA,Kucera SU,Williams RO 3rd

doi

10.1208/s12249-018-0988-1

subject

Has Abstract

pub_date

2018-07-01 00:00:00

pages

1957-1970

issue

5

issn

1530-9932

pii

10.1208/s12249-018-0988-1

journal_volume

19

pub_type

杂志文章
  • Novel biodegradable polyester poly(propylene succinate): synthesis and application in the preparation of solid dispersions and nanoparticles of a water-soluble drug.

    abstract::Poly(propylene succinate) (PPSu) polymers of average molecular weights from 2,800 to 13,100 g/mol were synthesized and characterized with regard to crystallinity, thermal properties, and cytocompatibility. Higher molecular weight samples exhibited lower degree of crystallinity and melted at lower temperatures. Melting...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-008-9184-z

    authors: Bikiaris DN,Papageorgiou GZ,Papadimitriou SA,Karavas E,Avgoustakis K

    更新日期:2009-01-01 00:00:00

  • Nucleic Acid-Based Therapeutics for Pulmonary Diseases.

    abstract::Nucleic acid-based therapeutics present huge potential in the treatment of pulmonary diseases ranging from lung cancer to asthma and chronic pulmonary diseases, which are often fatal and widely prevalent. The susceptibility of nucleic acids to degradation and the complex structure of lungs retard the effective pulmona...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章,评审

    doi:10.1208/s12249-018-1183-0

    authors: Chen J,Tang Y,Liu Y,Dou Y

    更新日期:2018-11-01 00:00:00

  • Isolation, Formulation, and Efficacy Enhancement of Morin Emulsified Carriers Against Lung Toxicity in Rats.

    abstract::The present study demonstrates a preparative medium-pressure liquid chromatography (MPLC) method for isolation of Morin besides evaluating its efficacy in comparison with its self-nanoemulsifying drug delivery (SNEDD) and nanoemulsion (NE) systems against in-vivo HgCl2-induced lung toxicity in rats. Morin was isolated...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-018-1072-6

    authors: El-Haddad AE,Sheta NM,Boshra SA

    更新日期:2018-07-01 00:00:00

  • Paul B. Myrdal, Ph.D. (June 25, 1967-May 19, 2018).

    abstract:: ...

    journal_title:AAPS PharmSciTech

    pub_type: 传,历史文章,新闻

    doi:10.1208/s12249-018-1106-0

    authors: Williams ROB 3rd

    更新日期:2018-08-01 00:00:00

  • An in vitro Assessment of Thermo-Reversible Gel Formulation Containing Sunitinib Nanoparticles for Neovascular Age-Related Macular Degeneration.

    abstract::Anti-vascular endothelial growth factor agents have been widely used to treat several eye diseases including age-related macular degeneration (AMD). An approach to maximize the local concentration of drug at the target site and minimize systemic exposure is to be sought. Sunitinib malate, a multiple receptor tyrosine ...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-019-1474-0

    authors: Bhatt P,Narvekar P,Lalani R,Chougule MB,Pathak Y,Sutariya V

    更新日期:2019-08-09 00:00:00

  • Preparation and evaluation of dermal delivery system of griseofulvin containing vitamin E-TPGS as penetration enhancer.

    abstract::Griseofulvin, an antifungal agent, is a BCS class II drug slowly, erratically, and incompletely absorbed from the gastrointestinal tract in humans. The clinical failure of the conventional oral therapy of griseofulvin is most likely attributed to its poor solubility and appreciable inter- and intra-subject variation i...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章,随机对照试验

    doi:10.1208/s12249-011-9722-y

    authors: Aggarwal N,Goindi S,Mehta SD

    更新日期:2012-03-01 00:00:00

  • Spray-Dried Succinylated Soy Protein Microparticles for Oral Ibuprofen Delivery.

    abstract::The potential value of succinylated soy protein (SPS) as a wall material for the encapsulation of ibuprofen (IBU), a model hydrophobic drug, by spray-drying was investigated. A succinylation rate of 93% was obtained for soy protein isolate, with a molar ratio of 1/1.5 (NH2/succinic anhydride). The solubility profile a...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-018-1250-6

    authors: Anaya Castro MA,Alric I,Brouillet F,Peydecastaing J,Fullana SG,Durrieu V

    更新日期:2019-01-11 00:00:00

  • Application of near-infrared spectroscopy in real-time monitoring of product attributes of ribbed roller compacted flakes.

    abstract::This study assessed the utility of near-infrared (NIR) spectroscopy for the real-time monitoring of content uniformity and critical quality attributes (tensile strength, Young's modulus, and relative density) of ribbed roller compacted flakes made by axially corrugated or ribbed rolls. A custom-built setup was used to...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-012-9890-4

    authors: Samanta AK,Karande AD,Ng KY,Heng PW

    更新日期:2013-03-01 00:00:00

  • Direct compression behavior of low- and high-methoxylated pectins.

    abstract::The objective of this study was to evaluate possible usefulness of pectins for direct compression of tablets. The deformation behavior of pectin grades of different degree of methoxylation (DM), namely, 5%, 10%, 25%, 35%, 40%, 50%, and 60% were, examined in terms of yield pressures (YP) derived from Heckel profiles fo...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-009-9349-4

    authors: Salbu L,Bauer-Brandl A,Tho I

    更新日期:2010-03-01 00:00:00

  • Studies on mefenamic acid microparticles: formulation, in vitro release, and in situ studies in rats.

    abstract::In this study, we investigated the in vitro characteristics of mefenamic acid (MA) microparticles as well as their effects on DNA damage. MA-loaded chitosan and alginate beads were prepared by the ionotropic gelation process. Microsponges containing MA and Eudragit RS 100 were prepared by quasi-emulsion solvent diffus...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-008-9183-0

    authors: Sevgi F,Yurdasiper A,Kaynarsoy B,Turunç E,Güneri T,Yalçin A

    更新日期:2009-01-01 00:00:00

  • Formulation Optimization and Ex Vivo and In Vivo Evaluation of Celecoxib Microemulsion-Based Gel for Transdermal Delivery.

    abstract::Celecoxib (CXB) is a poorly aqueous solubility sulfonamide non-steroidal anti-inflammatory drug (NSAID). Hence, the formulation of CXB was selected for solubilization and bioavailability. To find out suitable formulation for microemulsion, the solubility of CXB in triacetin (oil phase), Tween 80 (surfactant), and Tran...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-016-0667-z

    authors: Cao M,Ren L,Chen G

    更新日期:2017-08-01 00:00:00

  • Screening of venlafaxine hydrochloride for transdermal delivery: passive diffusion and iontophoresis.

    abstract::The objective of the study was to investigate in vitro transdermal delivery of venlafaxine hydrochloride across the pigskin by passive diffusion and iontophoresis. For passive diffusion, experiments were carried out in Franz diffusion cell whereas for iontophoretic permeation, the diffusion cell was modified to contai...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-008-9111-3

    authors: Singh G,Ghosh B,Kaushalkumar D,Somsekhar V

    更新日期:2008-01-01 00:00:00

  • Pulmonary and Regional Deposition of Nebulized and Dry Powder Aerosols in Ferrets.

    abstract::The utilization of ferrets as a non-clinical model for disease is rapidly increasing within drug development. Many of these models include respiratory diseases that involve targeted drug delivery via nose-only inhalation. While the deposition patterns within other non-clinical models (mice, rats, canines, and non-huma...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-019-1382-3

    authors: Kuehl PJ,Chand R,McDonald JD,Hava DL,DeHaan WH

    更新日期:2019-07-01 00:00:00

  • Complex Drug Delivery Systems: Controlling Transdermal Permeation Rates with Multiple Active Pharmaceutical Ingredients.

    abstract::A transdermal drug delivery system (TDDS) is generally designed to deliver an active pharmaceutical ingredient (API) through the skin for systemic action. Permeation of an API through the skin is controlled by adjusting drug concentration, formulation composition, and patch design. A bilayer, drug-in-adhesive TDDS des...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-020-01682-4

    authors: Davis DA,Martins PP,Zamloot MS,Kucera SA,Williams RO 3rd,Smyth HDC,Warnken ZN

    更新日期:2020-06-04 00:00:00

  • The Localization of Phenolic Compounds in Liposomal Bilayers and Their Effects on Surface Characteristics and Colloidal Stability.

    abstract::The interactions with and effects of five chemically distinct, bioactive phenolic compounds on the lipid bilayers of model dipalmitoylphosphatidylcholine (DPPC) liposomes were investigated. Complementary analytical techniques, including differential scanning calorimetry (DSC) and phosphorus and proton nuclear magnetic...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-016-0483-5

    authors: Malekar SA,Sarode AL,Bach AC 2nd,Worthen DR

    更新日期:2016-12-01 00:00:00

  • The Sensitivity of In Vitro Permeation Tests to Chemical Penetration Enhancer Concentration Changes in Fentanyl Transdermal Delivery Systems.

    abstract::Chemical penetration enhancers (CPEs) are frequently incorporated into transdermal delivery systems (TDSs) to improve drug delivery and to reduce the required drug load in formulations. However, the minimum detectable effect of formulation changes to CPE-containing TDSs using in vitro permeation tests (IVPT), a widely...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-018-1130-0

    authors: Shin SH,Srivilai J,Ibrahim SA,Strasinger C,Hammell DC,Hassan HE,Stinchcomb AL

    更新日期:2018-10-01 00:00:00

  • Pluronic-Based Mixed Polymeric Micelles Enhance the Therapeutic Potential of Curcumin.

    abstract::Curcumin is a naturally occurring constituent of turmeric that is a good substitute for synthetic medicines for the treatment of different diseases, due to its comparatively safer profile. However, there are certain shortcomings that limit its use as an ideal therapeutic agent. In order to overcome these drawbacks, we...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-018-1098-9

    authors: Akbar MU,Zia KM,Nazir A,Iqbal J,Ejaz SA,Akash MSH

    更新日期:2018-08-01 00:00:00

  • Co-Processed Excipients for Dispersible Tablets-Part 2: Patient Acceptability.

    abstract::Palatability and patient acceptability are critical attributes of dispersible tablet formulation. Co-processed excipients could provide improved organoleptic profile due to rational choice of excipients and manufacturing techniques. The aim of this study was to identify the most suitable co-processed excipient to use ...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-018-1104-2

    authors: Dziemidowicz K,Lopez FL,Bowles BJ,Edwards AJ,Ernest TB,Orlu M,Tuleu C

    更新日期:2018-08-01 00:00:00

  • Inline real-time near-infrared granule moisture measurements of a continuous granulation-drying-milling process.

    abstract::The purpose of this research was to use inline real-time near-infrared (NIR) to measure the moisture content of granules manufactured using a commercial production scale continuous twin-screw granulator fluid-bed dryer milling process. A central composite response surface statistical design was used to study the effec...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-011-9669-z

    authors: Chablani L,Taylor MK,Mehrotra A,Rameas P,Stagner WC

    更新日期:2011-12-01 00:00:00

  • Percutaneous Delivery of Antihypertensive Agents: Advances and Challenges.

    abstract::Hypertension remains a significant risk factor for several cardiovascular disorders including coronary artery disease and heart failure. Despite the large armamentarium of drugs available for the management of high blood pressure, low oral availability is an ongoing challenge. Researchers are constantly developing alt...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章,评审

    doi:10.1208/s12249-019-1583-9

    authors: Ita K,Ashong S

    更新日期:2020-01-06 00:00:00

  • Effect of organogel components on in vitro nasal delivery of propranolol hydrochloride.

    abstract::The purpose of this research was to evaluate in vitro transnasal sustained-release ability of sorbitan monostearate (SMS) organogels in isopropyl myristate (IM). Organogels were prepared containing SMS (2.5%-20%) and water (5%-25%) in IM and analyzed microscopically for phase behavior. The effect of Tween surfactants ...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/pt050463

    authors: Pisal S,Shelke V,Mahadik K,Kadam S

    更新日期:2004-09-13 00:00:00

  • GM-144, a novel lipophilic vaginal contraceptive gel-microemulsion.

    abstract::In a systematic effort to develop a dual-function intravaginal spermicide as well as a drug delivery vehicle against sexually transmitted pathogens, a submicron particle size (30-80 nm), lipophilic and spermicidal gel-microemulsion (viz GM-144) containing the pharmaceutical excipients propylene glycol, Captex 300, Cre...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/pt020205

    authors: D'Cruz OJ,Yiv SH,Uckun FM

    更新日期:2001-04-09 00:00:00

  • Use of Risk Assessment and Plackett-Burman Design for Developing Resveratrol Spray-Dried Emulsions: a Quality-by-Design Approach.

    abstract::In this study, the resveratrol spray-dried emulsions were developed using a quality-by-design approach. Further, the product and process factors that affected the quality of the spray-dried emulsions were analyzed and illustrated using an Ishikawa diagram. The product and process risks were prioritized using a risk-ra...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-018-1220-z

    authors: Benjasirimongkol P,Piriyaprasarth S,Moribe K,Sriamornsak P

    更新日期:2018-12-18 00:00:00

  • Influence of process and formulation parameters on dissolution and stability characteristics of Kollidon® VA 64 hot-melt extrudates.

    abstract::The objective of the present study was to investigate the effects of processing variables and formulation factors on the characteristics of hot-melt extrudates containing a copolymer (Kollidon® VA 64). Nifedipine was used as a model drug in all of the extrudates. Differential scanning calorimetry (DSC) was utilized on...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-014-0226-4

    authors: Maddineni S,Battu SK,Morott J,Majumdar S,Murthy SN,Repka MA

    更新日期:2015-04-01 00:00:00

  • A new approach for increasing ascorbyl palmitate stability by addition of non-irritant co-antioxidant.

    abstract::The aim of this work was to test innovative approach for enhancing ascorbyl palmitate stability in microemulsions for topical application by addition of newly synthesized co-antioxidant 4-(tridecyloxy)benzaldehyde oxime (TDBO) and to investigate its antioxidant activity and finally to evaluate cytotoxicity of TDBO-loa...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-010-9507-8

    authors: Gosenca M,Obreza A,Pečar S,Gašperlin M

    更新日期:2010-09-01 00:00:00

  • Characterization and in vitro drug release studies of a natural polysaccharide Terminalia catappa gum (Badam gum).

    abstract::The main objective of the present study is the physicochemical characterization of naturally available Terminalia catappa gum (Badam gum [BG]) as a novel pharmaceutical excipient and its suitability in the development of gastroretentive floating drug delivery systems (GRFDDS) to retard the drug for 12 h when the dosag...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-012-9873-5

    authors: Meka VS,Nali SR,Songa AS,Kolapalli VR

    更新日期:2012-12-01 00:00:00

  • Development and evaluation of buccoadhesive controlled release tablets of lercanidipine.

    abstract::The purpose of this research was to develop and evaluate buccal mucoadhesive controlled release tablets of lercanidipine hydrochloride using polyethylene oxide and different viscosity grades of hydroxypropyl methylcellulose individually and in combination. Effect of polymer type, proportion and combination was studied...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-007-9031-7

    authors: Charde S,Mudgal M,Kumar L,Saha R

    更新日期:2008-01-01 00:00:00

  • Preparation and In Vitro-In Vivo Evaluation of Sustained-Release Matrix Pellets of Capsaicin to Enhance the Oral Bioavailability.

    abstract::Capsaicin has multiple pharmacological activities including antioxidant, anticancer, and anti-inflammatory activities. However, its clinical application is limited due to its poor aqueous solubility, gastric irritation, and low oral bioavailability. This research was aimed at preparing sustained-release matrix pellets...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-015-0352-7

    authors: Zhang Y,Huang Z,Omari-Siaw E,Lu S,Zhu Y,Jiang D,Wang M,Yu J,Xu X,Zhang W

    更新日期:2016-04-01 00:00:00

  • Supercritical assisted atomization: a novel technology for microparticles preparation of an asthma-controlling drug.

    abstract::The objective of this study was to produce microparticles of a new asthma-controlling drug by supercritical assisted atomization (SAA), proposed as an alternative to conventional jet-milling process. SAA is based on the solubilization of supercritical carbon dioxide in a liquid solution containing the drug; the ternar...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/pt060352

    authors: Della Porta G,De Vittori C,Reverchon E

    更新日期:2005-10-22 00:00:00

  • Data-Driven Modeling of the Bicalutamide Dissolution from Powder Systems.

    abstract::Low solubility of active pharmaceutical compounds (APIs) remains an important challenge in dosage form development process. In the manuscript, empirical models were developed and analyzed in order to predict dissolution of bicalutamide (BCL) from solid dispersion with various carriers. BCL was chosen as an example of ...

    journal_title:AAPS PharmSciTech

    pub_type: 杂志文章

    doi:10.1208/s12249-020-01660-w

    authors: Mendyk A,Pacławski A,Szafraniec-Szczęsny J,Antosik A,Jamróz W,Paluch M,Jachowicz R

    更新日期:2020-03-31 00:00:00