Dados Gerais do Componente Curricular
| Tipo do Componente Curricular: |
MÓDULO |
| Unidade Responsável: |
PROGRAMA DE PÓS-GRADUAÇÃO EM CIÊNCIAS DA SAÚDE (15.26) |
| Código: |
PPGCSA0019 |
| Nome: |
NEW TRENDS IN HEALTH SCIENCES - INSIGHTS ON OILY SOLUTIONS OR DISPERSIONS AS THERAPEUTICAL PRODUCTS |
| Carga Horária Teórica: |
30 h. |
| Carga Horária Prática: |
0 h. |
| Carga Horária de Ead: |
0 h. |
| Carga Horária Total: |
30 h. |
| Pré-Requisitos: |
|
| Co-Requisitos: |
|
| Equivalências: |
|
| Excluir da Avaliação Institucional: |
Não |
| Matriculável On-Line: |
Sim |
| Método de Avaliação: |
CONCEITO |
| Horário Flexível da Turma: |
Não |
| Horário Flexível do Docente: |
Sim |
| Obrigatoriedade de Nota Final: |
Sim |
| Pode Criar Turma Sem Solicitação: |
Não |
| Necessita de Orientador: |
Não |
| Exige Horário: |
Sim |
| Permite CH Compartilhada: |
Não |
| Permite Múltiplas Aprovações: |
Não |
| Quantidade de Avaliações: |
1 |
| Ementa/Descrição: |
Main Topic:“Drug delivery systems, from the bench to the industry”
Description:
Course Overview
This course explores cutting-edge trends in health sciences focusing on oily solutions and dispersions as therapeutic products. Students will gain insights into the challenges of formulating oily solutions, the physicochemical properties essential for product stability, the quality control measures required for such formulations, and the criteria for selecting suitable Active Pharmaceutical Ingredients (APIs) for these carriers.
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Objectives
By the end of this course, students will be able to:
1. Identify and address challenges in the development of oily solutions and dispersions.
2. Analyze the physicochemical principles underlying formulation stability.
3. Design quality control protocols for medicines containing oily formulations.
4. Evaluate potential molecules for delivery via oily solutions based on their characteristics.
Course design: The course duration is one semester with a Week Modulus, five days of around 6 hours classes per day. Each day will begin with one lecturefollowed by case studies using recent publications on the topic. The covering of three main areas of drug development will be presented by three different teachers. Students will then be assigned workshop problems to provide them with an active learning application of the |
| Referências: |
Main References
Larsen C, Larsen SW, Jensen H, Yaghmur A, Ostergaard J. Role of in vitro release models in formulation development and quality control of parenteral depots. Expert Opin Drug Deliv.6(12):1283-95 (2009). doi: 10.1517/17425240903307431. PMID: 19941410.
Reddy, M.R., Gubbiyappa, K.S. Formulation Development, Optimization, and Characterization of Entrectinib-Loaded Supersaturable Self-Nanoemulsifying Drug Delivery Systems. BioNanoSci.13: 521–540 (2023). https://doi.org/10.1007/s12668-023-01094-1
Ali, Heyam. A Comprehensive Review in Parenteral Formulations. Acta Scientific Pharmaceutical Sciences. 4: 33-41(2020). 10.31080/ASPS.2020.04.0554.
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