Joana Marto
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Joana Marto has a total of 388 co-authors. Here are the top co-authors by number of shared publications:
- Helena Margarida Ribeiro
Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Professor Gama Pinto, 1649-003 Lisboa, Portugal
90 shared publications - Luis Miguel Goncalves
Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Avenida Professor Gama Pinto, 1649-038 Lisboa, Portugal
40 shared publications - Ana Margarida Martins
Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Professor Gama Pinto, 1649-003 Lisboa, Portugal
26 shared publications - António José Almeida
Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Professor Gama Pinto, 1649-003 Lisbon, Portugal
25 shared publications - Sandra Simões
Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa
24 shared publications - Pedro Pinto
Research Institute for Medicines (iMed.ULisboa), Faculdade de Farmácia, Universidade de Lisboa, Lisbon, Portugal
19 shared publications
Latest Publications
- 1 October 2026
- Published by Springer Nature in Phytochemistry Reviews
- p. 1-31
Valorization of industrial byproducts for cosmetic ingredients: deep eutectic solvents as a greener alternative
- 1 October 2026
- Published by Springer Nature in Phytochemistry Reviews
- p. 1-31
Valorization of industrial byproducts for cosmetic ingredients: deep eutectic solvents as a greener alternative
- Open Access
- 23 September 2026
- Published by Elsevier in Applied Food Research
- Vol. 6 (2)
From olive leaves to film-forming hydrogels: Optimisation of microwave-assisted extraction and formulation characterisation
- 23 September 2026
- Published by Elsevier in Applied Food Research
- Vol. 6 (2)
Open AccessFrom olive leaves to film-forming hydrogels: Optimisation of microwave-assisted extraction and formulation characterisation
- Open Access
- 12 September 2026
- Published by Elsevier in Journal of Drug Delivery Science and Technology
- Vol. 127
Development of a novel in situ foamed tomatine formulation for cutaneous inflammation management
- 12 September 2026
- Published by Elsevier in Journal of Drug Delivery Science and Technology
- Vol. 127
Open AccessDevelopment of a novel in situ foamed tomatine formulation for cutaneous inflammation management
- Open Access
- 13 August 2026
- Published by Elsevier in Currents in Pharmacy Teaching and Learning
- Vol. 18 (12)
Implementing emerging 3D printing technologies into pharmaceutical sciences education: Pedagogical strategies and learning outcomes
- 13 August 2026
- Published by Elsevier in Currents in Pharmacy Teaching and Learning
- Vol. 18 (12)
Open AccessImplementing emerging 3D printing technologies into pharmaceutical sciences education: Pedagogical strategies and learning outcomes
- Open Access
- 11 June 2026
- Published by Springer Nature in AAPS PharmSciTech
- Vol. 27 (5)
Chloramphenicol Application Onto the Eyelid: Transfersomes for Enhanced Skin Delivery
The aim of the study was to prepare chloramphenicol (CAM)-loaded transfersomes to enhance drug permeability following topical administration, considering the final goal of treating conjunctivitis by applying the formulation onto the eyelid. The CAM-loaded transfersomes obtained have an average particle size of approximately 120 nm, are monodispersed with polydispersity index < 0.1, and exhibit high encapsulation efficiency (84 ± 5.5%). The formulation showed vesicle deformability, good biocompatibility and enhanced skin permeation compared to a conventional ophthalmic formulation of the antibiotic. The optimized drug-loaded nanosystem was subsequently jellified and the fluid gel obtained presented rheological behaviour adequate for application onto the eyelid. The formulation showed physical and chemical stability after 3 months storage. Therefore, eyelid administration of CAM-loaded transfersomes could be considered as a potential strategy for the treatment of bacterial conjunctivitis.
- 11 June 2026
- Published by Springer Nature in AAPS PharmSciTech
- Vol. 27 (5)
Open AccessChloramphenicol Application Onto the Eyelid: Transfersomes for Enhanced Skin Delivery
The aim of the study was to prepare chloramphenicol (CAM)-loaded transfersomes to enhance drug permeability following topical administration, considering the final goal of treating conjunctivitis by applying the formulation onto the eyelid. The CAM-loaded transfersomes obtained have an average particle size of approximately 120 nm, are monodispersed with polydispersity index < 0.1, and exhibit high encapsulation efficiency (84 ± 5.5%). The formulation showed vesicle deformability, good biocompatibility and enhanced skin permeation compared to a conventional ophthalmic formulation of the antibiotic. The optimized drug-loaded nanosystem was subsequently jellified and the fluid gel obtained presented rheological behaviour adequate for application onto the eyelid. The formulation showed physical and chemical stability after 3 months storage. Therefore, eyelid administration of CAM-loaded transfersomes could be considered as a potential strategy for the treatment of bacterial conjunctivitis.
- Open Access
- 22 April 2026
- Published by Elsevier in Materials Today Communications
- Vol. 52
Novel skin-compatible gelatin methacrylate-tannic acid hydrogel resin for photocrosslinkable 3D printing applications
- 22 April 2026
- Published by Elsevier in Materials Today Communications
- Vol. 52
Open AccessNovel skin-compatible gelatin methacrylate-tannic acid hydrogel resin for photocrosslinkable 3D printing applications
- Open Access
- 10 April 2026
- Published by Elsevier in International Journal of Pharmaceutics
- Vol. 697, 126863
Print, check, repeat: digital quality by design for 3D-printed medicines using OpenAI models
- 10 April 2026
- Published by Elsevier in International Journal of Pharmaceutics
- Vol. 697, 126863
Open AccessPrint, check, repeat: digital quality by design for 3D-printed medicines using OpenAI models
- Open Access
- 11 March 2026
- Published by Elsevier in International Journal of Pharmaceutics
- Vol. 694, 126750
Beyond spectroscopy: Machine vision as the future of non-destructive testing in 3D-printed pharmaceuticals
- 11 March 2026
- Published by Elsevier in International Journal of Pharmaceutics
- Vol. 694, 126750
Open AccessBeyond spectroscopy: Machine vision as the future of non-destructive testing in 3D-printed pharmaceuticals
- Open Access
- 10 March 2026
- Published by MDPI AG in Pharmaceuticals
- Vol. 19 (3) , 447
Valorization of Olive Stones: Chemical Composition and Bioactivity
Background/Objectives: The consumption of olive oil and olives has been steadily increasing, leading to growing interest in the sustainable management of by-products such as olive stones. This work aimed to contribute to the development of valorization strategies by studying the chemical composition and biological potential of olive stone extracts, using both conventional and eco-friendly extraction methods with various solvents. Methods: Several extracts were prepared and chemically characterized regarding their fatty acid and phenolic profiles by GC-FID and HPLC-DAD-MS/MS, respectively. Their antioxidant, cytotoxic and antiproliferative activities were also evaluated. Results: n-Hexane Soxhlet extract yielded higher concentrations and a broader range of fatty acids when compared to the chloroform-methanol Folch extract. Oleic, palmitic, and linoleic acids were the predominant fatty acids in the extracts. A large variety of phenolic compounds were identified in extracts obtained by microwave-assisted extraction (MAE), including several flavonoids, small phenolic compounds, secoiridoids (nuezhenide and oleuropein), and hydroxytyrosol. MAE hydroalcoholic extracts showed high total phenolic content (TPC), antioxidant activity by the oxygen radical absorption capacity (ORAC) and hydroxyl radical scavenging capacity (HOSC) assays. Moreover, the aqueous ethanol (50%) and aqueous methanol (80%) extracts displayed low cytotoxicity toward the non-malignant Caco-2 cell line (IC50 values of 1.29 and 1.40 mg/mL, respectively), while both induced complete loss of viability in the HT-29 human colon adenocarcinoma cell line at 0.63 mg/mL. Conclusions: These findings highlight the potential of olive stone as a valuable source of bioactive compounds with antioxidant and selective antiproliferative properties. The results support their further exploration in the development of sustainable valorization strategies for olive industry by-products.
- 10 March 2026
- Published by MDPI AG in Pharmaceuticals
- Vol. 19 (3) , 447
Open AccessValorization of Olive Stones: Chemical Composition and Bioactivity
Background/Objectives: The consumption of olive oil and olives has been steadily increasing, leading to growing interest in the sustainable management of by-products such as olive stones. This work aimed to contribute to the development of valorization strategies by studying the chemical composition and biological potential of olive stone extracts, using both conventional and eco-friendly extraction methods with various solvents. Methods: Several extracts were prepared and chemically characterized regarding their fatty acid and phenolic profiles by GC-FID and HPLC-DAD-MS/MS, respectively. Their antioxidant, cytotoxic and antiproliferative activities were also evaluated. Results: n-Hexane Soxhlet extract yielded higher concentrations and a broader range of fatty acids when compared to the chloroform-methanol Folch extract. Oleic, palmitic, and linoleic acids were the predominant fatty acids in the extracts. A large variety of phenolic compounds were identified in extracts obtained by microwave-assisted extraction (MAE), including several flavonoids, small phenolic compounds, secoiridoids (nuezhenide and oleuropein), and hydroxytyrosol. MAE hydroalcoholic extracts showed high total phenolic content (TPC), antioxidant activity by the oxygen radical absorption capacity (ORAC) and hydroxyl radical scavenging capacity (HOSC) assays. Moreover, the aqueous ethanol (50%) and aqueous methanol (80%) extracts displayed low cytotoxicity toward the non-malignant Caco-2 cell line (IC50 values of 1.29 and 1.40 mg/mL, respectively), while both induced complete loss of viability in the HT-29 human colon adenocarcinoma cell line at 0.63 mg/mL. Conclusions: These findings highlight the potential of olive stone as a valuable source of bioactive compounds with antioxidant and selective antiproliferative properties. The results support their further exploration in the development of sustainable valorization strategies for olive industry by-products.