Journal of Bioequivalence & Bioavailability

Journal of Bioequivalence & Bioavailability
Open Access

ISSN: 0975-0851

+44 7480022449

Citations Report

Citations Report - Journal of Bioequivalence & Bioavailability [817 Articles]

The articles published in Journal of Bioequivalence & Bioavailability have been cited 817 times by eminent researchers all around the world. Following is the list of articles that have cited the articles published in Journal of Bioequivalence & Bioavailability.

Vadlamudi MK, Dhanaraj S (2016) Disparate practical way of doing solubility enhancement study to improve the bioavailability of poorly soluble drugs. J Chem Pharm Res 8:208-235.

Patel AR, Godugu C, Wilson H, Safe S, Singh M (2015) Evaluation of spray BIO-Max DIM-P in dogs for oral bioavailability and in nu/nu mice bearing orthotopic/metastatic lung tumor models for anticancer activity. Pharm Res 32:2292-2300.

Rahman MM, Khalipha AB, Azad MA, Hossain S, Haque S (2014) Methods of solubility and dissolution enhancement for poorly water soluble drugs: a review. World J Pharm Pharm Sci 3:107-130.

Price DJ, Ditzinger F, Koehl NJ, Jankovic S, Tsakiridou G, Nair A, et al. (2019) Approaches to increase mechanistic understanding and aid in the selection of precipitation inhibitors for supersaturating formulations–a PEARRL review. J Pharm Pharma 71:483-509.

Boroujeni HC, Gharib F (2016) Solvatochromism and preferential solvation of deferiprone in some water–organic mixed solvents. J Sol Chem 45:95-108.

Berardi A, Bisharat L (2014) Nanotechnology systems for oral drug delivery: challenges and opportunities. Nanotechnol Drug Deliv 3:52-84.

Hunter CA, Prohens R (2017) Solid form and solubility. CrystEngComm 19:23-26.

Seo JH, Park JB, Choi WK, Park S, Sung YJ, Oh E, et al. () Improved oral absorption of cilostazol via sulfonate salt formation with mesylate and besylate. Drug Design Develop Ther 9:3961.

Ahmed AB, Konwar R, Sengupta R (2015) Atorvastatin calcium loaded chitosan nanoparticles: in vitro evaluation and in vivo pharmacokinetic studies in rabbits. Brazilian J Pharm Sci 51:467-477.

Ahmed TA, Khalid M (2016) Transdermal film-loaded finasteride microplates to enhance drug skin permeation: two-step optimization study. European J Pharm Sci 88:246-256.

Parthasarathi D, Gajendra C, Dattatreya A, Sree Venkatesh Y (2011) Analysis of pharmacokinetic & pharmacodynamic models in oral and transdermal dosage forms. J Bioequiv Availab 3:268-276.

Ozeki T, Tagami T (2013) Functionally engineered nanosized particles in pharmaceutics: improved oral delivery of poorly water-soluble drugs. Curr Pharm Design 19:6259-6269.

Vieira AC, Fontes DA, Chaves LL, Alves LD, de Freitas Neto JL, Soares MF, et al. (2015) Multicomponent systems with cyclodextrins and hydrophilic polymers for the delivery of Efavirenz. Carbohyd Polymers 130:133-140.

Shamshina JL, Rogers RD (2014) Overcoming the problems of solid state drug formulations with ionic liquids. Therapeut Deliv 5:489-491.

Душкин АВ, Сунцова ЛП, Халиков СС (2012) Механохимическая технология для повышения растворимости лекарственных веществ. Фундаментальные исследования 2.

Wairkar SM, Gaud RS (2013) Solid dispersions: Solubility enhancement technique for poorly soluble drugs. Int J Res Pharma Biomed Sci 4:847.

Shergill M, Patel M, Khan S, Bashir A, McConville C (2016) Development and characterisation of sustained release solid dispersion oral tablets containing the poorly water soluble drug disulfiram. Int J Pharm 497:3-11.

Abuzar SM, Hyun SM, Kim JH, Park HJ, Kim MS, Park JS, et al. (2018) Enhancing the solubility and bioavailability of poorly water-soluble drugs using supercritical antisolvent (SAS) process. Int J Pharm 538:1-3.

Jain A, Thakur D, Ghoshal G, Katare OP, Singh B, Shivhare US (2016) Formation and functional attributes of electrostatic complexes involving casein and anionic polysaccharides: an approach to enhance oral absorption of lycopene in rats in vivo. Int J Biol Macromol 93:746-756.

Burak C, Brüll V, Langguth P, Zimmermann BF, Stoffel-Wagner B, Sausen U, et al. (2017) Higher plasma quercetin levels following oral administration of an onion skin extract compared with pure quercetin dihydrate in humans. European J Nutri 56:343-353.