• Aulton, Michael E; Tayor, Kevin; . Aulton's Pharmaceutics: The Design and Manufacture of Medicines, 4th edition, Churcill Livingstone, (2013) Prista, L.N., Alves, A.C. & Morgado, R. (2007). Tecnologia Farmacêutica. Lisboa: Fundação Calouste Gulbenkian. Pharmaceutical Formulation: The Science and Technology of Dosage Forms; Editor: Geoffrey D Tovey; Royal Society of Chemistry, 2018 Ministério da Saúde, Instituto Nacional da Farmácia e do Medicamento (INFARMED) (2010). Farmacopeia Portuguesa 9.8. Lisboa: Imprensa Nacional Casa da Moeda. Current version of European Pharmacopoeia (Ph. Eur.) (Council of Europe Convention) Current version of United States Pharmacopoeia and National Formulary (United States Pharmacopeial Convention,Inc.)  
  • Pharmacy
  • 4003
  • 19589
  • Pharmaceutical Technology
  • IPLUSO4003-19589
  • 3
  • 6
  • 0
  • 4
  • Não
  • Português
  • In this curricular unit, the Team-based learning (TBL) methodology is used, with tasks carried out in small groups, allowing the development of the ability to analyze and apply theoretical concepts.  
  • Mandatory
  • In this curricular unit, solid dosage forms for oral administration, injectable preparations, dosage forms for ophthalmic, nasal and auricular application, semi-solid dosage forms, rectal and vaginal dosage forms will be studied, as well as the respective quality control tests. The different types of packaging will also be presented as well as the impact they have on the aforementioned pharmaceutical forms. In the end, students should master the concepts and terminology used in Pharmaceutical Technology, thus acquiring scientific bases and essential skills for the development of their future professional activity.  At the end of this curricular unit the student must: - understand the different pharmaceutical dosage forms and the respective routes of administration; - understand the parameters used in pre-formulation studies; - distinguish and understand the role of excipients used in the formulation of dosage forms; - understand the quality control methods for each dosage form;
  • Pre-formulation studies in pharmaceutical technology for solid dosage forms. Solid dosage forms for oral administration. Preparations for ophthalmic application. Nasal preparations. Auricular preparation. Injectable preparations. Semisolid dosage forms. Solid dosage forms for rectal and vaginal administration. Sterilization.
  • Avaliação contínua

    Descrição

    Data limite

    Ponderação

    1º teste de avaliação Teórico

    dd-mm-yyyy

    25 %

    1º teste de avaliação Prático

    dd-mm-yyyy

    25 %

    2º teste de avaliação Teórico

    dd-mm-yyyy

    25 %

    2º teste de avaliação Prático

             dd-mm-yyyy

    25 %

    A classificação final (CF) da unidade curricular por avaliação contínua é obtida a partir das classificações obtidas na componente escrita (T) e na componente prática (PL). A componente Teórica consta de duas frequências escritas e é relativa aos conteúdos teóricos. A classificação mínima em cada frequência é de 8 valores. A componente prática consta de 2 momentos de avaliação práticos realizados durante as aulas laboratoriais, A classificação mínima de cada momento é de 8 valores. A classificação final é calculada a partir da seguinte fórmula: CF = 0,50 T + 0,50 PL. A classificação de todos os instrumentos de avaliação é expressa numa escala de 0 a 20 valores, sendo que o valor ponderado das classificações obtidas tem de ser igual ou superior a 9,5

     

     

  • Semestral
  • Pharmaceutical Technology is the area of knowledge that studies drugs considering the most appropriate dosage form for their administration. Thus, this curricular unit covers all the technological and scientific concepts necessary for the development and production of pharmaceutical dosage forms.