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Showing 1-20 of 48 results
  1. Formulating GML-1 Tablets Using the Harrington Desirability Function

    Features of using the generalized Harrington desirability function for the selection of a binder and lubricant for GML-1 ( N -benzyl- N -methyl-1-phenylpyrrolo[1,2-...

    D. I. Gavrilov, E. V. Blynskaya, ... K. V. Alekseev in Pharmaceutical Chemistry Journal
    Article 01 April 2024
  2. Quality by Design (QbD) Process Design

    Quality by design (QbD) principles have become widely adopted in the pharmaceutical industry to ensure consistent quality of products through their...
    Ajay Babu Pazhayattil, Sanjay Sharma, ... Marzena Ingram in Technology Transfer
    Chapter 2023
  3. Post-Alcohol Corn Dregs as a Pharmaceutical Source for Obtaining Nitrogen-Containing Betaines

    A method was developed for producing betaine hydrochlorides (with added pepsin) in the form of substances and tablets intended for use as drugs with...

    N. Sh. Kaisheva, A. Sh. Kaishev, M. V. Larsky in Pharmaceutical Chemistry Journal
    Article 07 May 2022
  4. Influence of Various Disintegrants on the Quality of Microcrystalline Cellulose Tablets

    The effects of the superdisintegrants sodium starch glycolate, croscarmellose sodium, polacrilin potassium Kyron T-314, and Amberlite IRP 88 on the...

    N. B. Demina, N. V. Bobkova, ... I. I. Krasnyuk in Pharmaceutical Chemistry Journal
    Article 15 November 2018
  5. Phytochemistry and Pharmaceutical Technology Studies on Monteverdia ilicifolia (Maytenus ilicifolia): a Traditionally Used Medicinal Plant

    Monteverdia ilicifolia (Mart. ex Reissek) Biral, Celastraceae (Syn. Maytenus ilicifolia Mart. ex Reissek), is used in Brazil as a folk medicine to...

    Gabriela de Carvalho Meirelles, Sara Elis Bianchi, ... Valquíria Linck Bassani in Revista Brasileira de Farmacognosia
    Article 03 October 2022
  6. Use of Two-Factor Dispersion Analysis for Studying the Pharmaceutical and Technological Properties of Tablets of GK-2 – bis-(N-Monosuccinyl-L-Glutamyl-L-Lysine) Hexamethyleneamide, Dispersed in the Oral Cavity

    The influence of the type and ratio of co-process fillers and lubricating excipients on the properties of the final dosage form was studied during...

    S. V. Tishkov, E. V. Blynskaya, ... V. V. Bueva in Pharmaceutical Chemistry Journal
    Article 01 January 2022
  7. New Formulation Technique for Solubility and Dissolution Rate Enhancement of Poorly Soluble Drugs

    Ebastine (EBS) is a second-generation non-sedating antihistamine used for the prevention and treatment of allergic rhinitis and chronic idiopathic...

    Divya Harmalkar, Soraiya Godinho, ... Rupesh Kalidas Shirodkar in Pharmaceutical Chemistry Journal
    Article 01 November 2019
  8. Development and Study of Anxiolytic Effect of Gml-1 Tablet Dosage Form

    Novel pyrrolo[1,2- a ]pyrazine ligands of 18-kDa translocator protein (TSPO) were synthesized at Zakusov Research Institute of Pharmacology....

    M. A. Yarkova, E. V. Blynskaya, ... K. V. Alekseev in Pharmaceutical Chemistry Journal
    Article 11 July 2019
  9. Physicochemical and Technological Characteristics of Lycopus Europaeus L. Dry Herbal Extract and Related Compositions

    The physicochemical and technological properties of Lycopus europaeus dry herbal extract were studied. Excipients were also selected. The...

    O. A. Semkina, V. I. Zvereva, ... A. S. Khomik in Pharmaceutical Chemistry Journal
    Article 01 September 2019
  10. Oral Solids

    This chapter provides the pharmaceutical basis of common solid dosage forms and discusses biopharmaceutical aspects related to their formulation....
    Boy van Basten in Practical Pharmaceutics
    Chapter 2023
  11. Compatibility of Medicinal and Excipient Substances in the Development of Medicinal Formulations

    Attention is drawn to a contradiction associated with assessments of the compatibility of medicinal (MS) and excipient (ES) substances: that ES and...

    Article 31 October 2018
  12. Current Trends in the Development of Technologies for Matrix Formulations with Modified Release (Review)

    Current aspects of the technology used to create matrix formulations ar presented. The main types of matrix are described depending on their behavior...

    Article 01 October 2016
  13. Investigation on the effect of polymer and starch on the tablet properties of lyophilized orally disintegrating tablet

    Orally disintegrating tablet (ODT) is a user friendly and convenient dosage form. The study aimed to investigate the effect of polymers and wheat...

    Kai Bin Liew, Kok Khiang Peh in Archives of Pharmacal Research
    Article 13 January 2015
  14. Oral Solids

    This chapter provides the pharmaceutical basis of common solid dosage forms and discusses biopharmaceutical aspects related to their formulation....
    Minna Helin-Tanninen, João Pinto in Practical Pharmaceutics
    Chapter 2015
  15. Improved dosage form of the combined alendronate and calcitriol (Maxmarvil®) on the absorption of alendronate in Korean postmenopausal women

    Alendronate is one of the most potent anti-osteoporotic agents for postmenopausal osteoporosis. However, high doses of alendronate cause esophageal...

    Yoon-Sok Chung, Yong Jun Choi, So Hee Kim in Archives of Pharmacal Research
    Article 17 May 2013
  16. Development and evaluation of self-microemulsifying liquid and granule formulations of Brucea javanica oil

    The aim of this study was to develop and characterize a self-microemulsifying drug delivery system (SMEDDS) of Brucea javanica oil (BJO) and...

    Ali Shao, Gang Chen, ... Shaoyang Wei in Archives of Pharmacal Research
    Article 18 April 2013
  17. Formulation and in vivo evaluation of ondansetron orally disintegrating tablets using different superdisintegrants

    The aim of this study was to formulate cost effective taste-masked orally disintegrating tablets of ondansetron, a bitter drug using different...

    Ravi Sheshala, Nurzalina Khan, ... Yusrida Darwis in Archives of Pharmacal Research
    Article 01 November 2011
  18. Preparation and evaluation of pectin-based colon-specific pulsatile capsule in vitro and in vivo

    The purpose of this study was to develop and evaluate a colon-specific, pulsatile drug delivery system, which consists of an impermeable capsule body...

    **g Liu, Liangke Zhang, ... Huiming Jiang in Archives of Pharmacal Research
    Article 01 November 2012
  19. Formulation, development, and performance evaluation of metoclopramide HCl oro-dispersible sustained release tablet

    The present study was undertaken to develop and evaluate an oro-dispersible, sustained release tablet of metoclopramide HCl. The technology was...

    Nikhil Kasliwal, Jeetendra Singh Negi, ... Rahul Jain in Archives of Pharmacal Research
    Article 01 October 2011
  20. Comparative study of telmisartan tablets prepared via the wet granulation method and pritor™ prepared using the spray-drying method

    The wet granulation method was successfully used to manufacture amorphous telmisartan tablets (CNU) for comparison with the spray-drying method, used...

    Junsung Park, Hee Jun Park, ... Sung-Joo Hwang in Archives of Pharmacal Research
    Article 01 March 2011
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