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Current approaches in Lipidic-nanoparticle Systems for Buccal Drug Delivery

Publikováno v: Research Journal of Pharmacy and Technology. :1353-1358

The sublingual and buccal routes of administration have significant advantages for both local and systemic drug delivery. They have shown to be an effective alternative to the traditional oral route, especially when fast onset of action is required.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ec5fe4ab765ec1292f693a4b3d0fd065
https://doi.org/10.52711/0974-360x.2022.00226

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Paliperidone-benzamide Cocrystals: Preparation, Characterization, In Vitro/In Vivo Evaluation

Autor: Radha Rani Earle, G V RADHA

Publikováno v: Nanoscience & Nanotechnology-Asia. 12

Background: The current investigation contributes to the development of novel Paliperidone (PPD) co-crystals (CCs) using benzamide (BZ) as a conformer. The CCs were synthesized using the solvent evaporation technique. Methods: The enhancement in solu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5b69457472cae3922e096554e3386b08
https://doi.org/10.2174/2210681213666221031150449

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Formulation and Evaluation of Lignocaine Hydrochloride Proniosomes Loaded Orabase for Dental Anaesthesia

Autor: G V R L Soujanya, Sunayana N, Ganesh Sai Myneni, G V Radha, Charan K

Publikováno v: Journal of Drug Delivery and Therapeutics. 11:27-34

The aim of this research is to prepare and evaluate lignocaine HCl Proniosomal orabase for enhanced permeation and prolonged dental anaesthesia effect. Objective: Various lignocaine proniosomal gels were formulated employing various surfactants. Meth

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::70829d80da10d2430836989c40068e7e
https://doi.org/10.22270/jddt.v11i3-s.4866

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TOPICAL DRUG DELIVERY OF GOSSYPIN FROM PRONIOSOMAL GEL FORMULATIONS: IN VITRO EFFICACY AGAINST HUMAN MELANOMA CELLS

Autor: G. V. Radha, S. Ganapaty, Jampala Rajkumar

Publikováno v: International Journal of Applied Pharmaceutics. :144-152

Objective: This work aimed to establish and formulate the gossypinproniosomal gel drug delivery system. Methods: Gossypin-loaded proniosomal gels (GPG) was prepared using specific non-ionic surfactants (Spans), followed by particle size (PS), entrapm

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c30f17c51c647be3d1444ed3b4658417
https://doi.org/10.22159/ijap.2021v13i1.39609

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Insights into Novel Excipients of Self-Emulsifying Drug Delivery Systems and Their Significance: An Updated Review

Autor: G V Radha, Earle Radha Rani

Publikováno v: Critical Reviews™ in Therapeutic Drug Carrier Systems. 38:27-74

Self-emulsifying drug delivery system (SEDDS), a category of lipid-based technology, has gained interest in the recent years for enhancement of solubility and bioavailability of poorly water-soluble drugs. With the progress of research in this field,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46812dda702c0b5a96caedab76fd0d45
https://doi.org/10.1615/critrevtherdrugcarriersyst.2020034975

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Invivo Pharmacokientic and Pharamacodynamic Studies of Optimized Antihyperlipidemic Drug Loaded Solid Lipid Nanoparticle

Autor: Brito Raj S, G V Radha, Krishnaji Rao M, Gannimani Veerabhadra Rao, Bhaskar Reddy K

Publikováno v: International Journal of Research in Pharmaceutical Sciences. 11:7454-7463

The purpose of this research is to increase bioavailability by solid lipid nanoparticle (SLN) carrier for low bioavailable drugs (< 5%) such as Lovastatin. Eight SLN loaded Lovastatin was designed and optimised by variables such as Particle Size (PS

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3230c39bcebb806efce78e207346ccdc
https://doi.org/10.26452/ijrps.v11i4.3935

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DEVELOPMENT OF SELF NANO-EMULSIFYING DRUG DELIVERY SYSTEM FOR AN ANTI-HYPERTENSIVE AGENT FELODIPINE: A SYSTEMATIC APPROACH FOR LIPID NANO-FORMULATION WITH IMPROVED ORAL BIOAVAILABILITY IN RATS

Autor: G. V. Radha, K. Trideva Sastri

Publikováno v: International Journal of Applied Pharmaceutics. :86-94

Objective: The present study involves the development of SNEDDS employing essential oils for enhancing biopharmaceutical performance. Methods: Preliminary investigations suggested the selection of cinnamon oil as an essential oil, tween 60 as a surfa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::21ad79fa10e8cc9471cf15a8666948fa
https://doi.org/10.22159/ijap.2020v12i3.37203

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Akademický článek

Development and in-vivo evaluation of dry powders for reconstitution of solubility enhanced derivative of azithromycin dihydrate.

Autor: MADDUKURI, SRAVYA¹ sravya.maddukuri23@gmail.com, G. V., RADHA²

Publikováno v: International Journal of Pharmaceutical Research (09752366). Jul-Sep2019, Vol. 11 Issue 3, p1137-1153. 17p.

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FORMULATION DEVELOPMENT AND EVALUATION OF SUSTAINED RELEASE GASTRORETENTIVE TABLET OF EMTRICITABINE

Autor: B. Likhitha, K. Trideva Sastri, G. V. Radha, N. Manaswin

Publikováno v: International Journal of Applied Pharmaceutics. :236-240

Objective: The study aims for the design and evaluation of floating tablets of emtricitabine (EMT), post oral administration to sustain the release and enhance gastric residence time (GRT). Methods: EMT is a nucleoside reverse-transcriptase inhibitor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::51b3f7209c456db7185613ccfd04e103
https://doi.org/10.22159/ijap.2019v11i5.34840

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