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      Challenges to improve the biopharmaceutical properties of poorly water-soluble drugs and the application of the solid dispersion technology

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          Abstract

          ABSTRACT The oral solid dosage forms are extremely relevant to drug therapy and responsible for much of the pharmaceutical industry turnover worldwide. However, the development of medicines in solid form involves significant challenges, including obtaining formulations with appropriate bioavailability for low aqueous solubility drugs (classes II and IV of the Biopharmaceutics Classification System). One of the most effective strategies to overcome poor dissolution rate and low absorption of drugs is the solid dispersion technique, however, although it has been the focus of much research in recent decades, there are relatively few commercially available products based on such technology. This is mainly due to problems related to production scale-up and physicochemical instability and creates opportunities for new studies to explore the full potential of the technology. This review presents an overall approach to the factors affecting the dissolution rate and oral bioavailability of BCS-classes II and IV drugs and a brief review of the state-of-theart of solid dispersion technology.

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          Drug-like properties and the causes of poor solubility and poor permeability

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            Insoluble drug delivery strategies: review of recent advances and business prospects

            The emerging trends in the combinatorial chemistry and drug design have led to the development of drug candidates with greater lipophilicity, high molecular weight and poor water solubility. Majority of the failures in new drug development have been attributed to poor water solubility of the drug. Issues associated with poor solubility can lead to low bioavailability resulting in suboptimal drug delivery. About 40% of drugs with market approval and nearly 90% of molecules in the discovery pipeline are poorly water-soluble. With the advent of various insoluble drug delivery technologies, the challenge to formulate poorly water soluble drugs could be achieved. Numerous drugs associated with poor solubility and low bioavailabilities have been formulated into successful drug products. Several marketed drugs were reformulated to improve efficacy, safety and patient compliance. In order to gain marketing exclusivity and patent protection for such products, revitalization of poorly soluble drugs using insoluble drug delivery technologies have been successfully adopted by many pharmaceutical companies. This review covers the recent advances in the field of insoluble drug delivery and business prospects.
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              Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: basic approaches and practical applications.

              The poor oral bioavailability arising from poor aqueous solubility should make drug research and development more difficult. Various approaches have been developed with a focus on enhancement of the solubility, dissolution rate, and oral bioavailability of poorly water-soluble drugs. To complete development works within a limited amount of time, the establishment of a suitable formulation strategy should be a key consideration for the pharmaceutical development of poorly water-soluble drugs. In this article, viable formulation options are reviewed on the basis of the biopharmaceutics classification system of drug substances. The article describes the basic approaches for poorly water-soluble drugs, such as crystal modification, micronization, amorphization, self-emulsification, cyclodextrin complexation, and pH modification. Literature-based examples of the formulation options for poorly water-soluble compounds and their practical application to marketed products are also provided. Classification of drug candidates based on their biopharmaceutical properties can provide an indication of the difficulty of drug development works. A better understanding of the physicochemical and biopharmaceutical properties of drug substances and the limitations of each delivery option should lead to efficient formulation development for poorly water-soluble drugs. Copyright © 2011 Elsevier B.V. All rights reserved.
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                Author and article information

                Contributors
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Journal
                rmat
                Matéria (Rio de Janeiro)
                Matéria (Rio J.)
                Rede Latino-Americana de Materiais (Rio de Janeiro, RJ, Brazil )
                1517-7076
                December 2018
                : 23
                : 4
                : e12224
                Affiliations
                [01] Joinville orgnameUniversidade da Região de Joinville orgdiv1Programa de Pós-Graduação em Saúde e Meio Ambiente Brazil
                [02] Florianópolis Santa Catarina orgnameUniversidade Federal de Santa Catarina orgdiv1Programa de Pós-Graduação em Farmácia Brazil
                [03] Joinville orgnameUniversidade da Região de Joinville orgdiv1Departamento de Farmácia Brazil
                Article
                S1517-70762018000400415
                10.1590/s1517-707620180004.0558
                d38daac8-a47c-4ef0-b2e7-41ca3dca053a

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 19 November 2017
                : 15 June 2018
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 54, Pages: 0
                Product

                SciELO Brazil

                Categories
                Articles

                oral delivery,drug solubility,drug dissolution,solid dispersion

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