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Pharmaceutics
Special Issues
Emerging Strategies to Improve the Design and Manufacturing of Biocompatible...
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Emerging Strategies to Improve the Design and Manufacturing of Biocompatible Therapeutic Materials, 2nd Edition

A special issue of Pharmaceutics (ISSN 1999-4923). This special issue belongs to the section "Pharmaceutical Technology, Manufacturing and Devices".

Deadline for manuscript submissions: closed (30 September 2023) | Viewed by 1323

Special Issue Editors

Dr. Ana Alcudia

E-Mail Website
Guest Editor
Department of Organic and Medicinal Chemistry, Faculty of Pharmacy, University of Seville, C/Profesor García González, 2, 41012 Seville, Spain
Interests: coating materials; materials for prosthesis; polymers or gels for biomedicine; synthesis of potentially bioactive entities; modeling and drug delivery
Special Issues, Collections and Topics in MDPI journals
Dr. Belén Begines

E-Mail Website
Guest Editor
Department of Organic and Medicinal Chemistry, Faculty of Pharmacy, University of Seville. C/ Profesor Garcia Gonzalez, 2, 41012 Seville, Spain
Interests: polymer chemistry; biodegradable polymers; drug delivery systems; inkjet 3D printing; additive manufacturing
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Currently, the field of medicine is drastically increasing its results, mainly due to the progress in emerging areas such as nanomedicine, regenerative medicine, and personalized medicine. For example, the development of novel drug delivery systems in the form of nanoparticles is improving the LADME (liberation, absorption, distribution, metabolism and excretion) properties of the derived formulations, with a consequent enhancement of the treatment efficacy, a reduction in the secondary effects, and a better compliance with the dosage guidelines. On the other hand, the utilization of biocompatible scaffolds is translating into the possibility of regenerating biological tissues. Additionally, personalized medicine is benefiting from the advantages offered by additive manufacturing. However, all these areas have in common the need to develop novel materials or composites that fulfill the requirements of each application.

Therefore, this Special Issue aims to identify novel materials/composites that have been developed with specific characteristics to accomplish the biomedical application for which they were designed.

Dr. Ana Alcudia
Dr. Belén Begines
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Pharmaceutics is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2900 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • personalized medicine
  • nanomedicine
  • controlled release
  • antibacterial/antimicrobial activity
  • biodegradable hydrogels
  • micro and nanoparticles
  • biomaterials
  • biodegradable polymers
  • biocompatible coatings
  • nanocomposites
  • porous materials
  • modelling
  • encapsulation
  • additive manufacturing
  • 3D printing
  • prothesis
  • scaffolds
  • tissue targeting

Published Papers (1 paper)

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Research

30 pages, 7496 KiB  
Article
Antiproliferative Imidazo-Pyrazole-Based Hydrogel: A Promising Approach for the Development of New Treatments for PLX-Resistant Melanoma
by Silvana Alfei, Marco Milanese, Chiara Brullo, Giulia Elda Valenti, Cinzia Domenicotti, Eleonora Russo and Barbara Marengo
Pharmaceutics 2023, 15(10), 2425; https://doi.org/10.3390/pharmaceutics15102425 - 4 Oct 2023
Cited by 1 | Viewed by 1171
Abstract
Aiming at developing a dermal formulation against melanoma, the synthesized imidazo-pyrazoles 2-phenyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid (3-methoxy-4-phenoxy-benzylidene)-hydrazide (4G) and 2-phenyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid (4-benzyloxy-3-methoxy-benzylidene)-hydrazide (4I) were screened on patient-isolated melanoma cells (MEOV NT) and on Vemurafenib (PLX4032)-resistant (MEOV PLX-R) ones. Since 4I on MEOV [...] Read more.
Aiming at developing a dermal formulation against melanoma, the synthesized imidazo-pyrazoles 2-phenyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid (3-methoxy-4-phenoxy-benzylidene)-hydrazide (4G) and 2-phenyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid (4-benzyloxy-3-methoxy-benzylidene)-hydrazide (4I) were screened on patient-isolated melanoma cells (MEOV NT) and on Vemurafenib (PLX4032)-resistant (MEOV PLX-R) ones. Since 4I on MEOV PLX-R cells was 1.4-fold more effective than PLX, a hydrogel formulation containing 4I (R4HG-4I) was prepared in parallel with an empty R4-based hydrogel (R4HG) using a synthesized antibacterial resin (R4) as gelling agent. Thanks to its high hydrophilicity, porosity (85%), and excellent swelling capability (552%), R4 allowed to achieve R4HG and R4HG-4I with high equilibrium degree of swelling (EDS) and equilibrium water content (EWC). Chemometric-assisted ATR-FTIR analyses confirmed the chemical structure of swollen and fully dried (R4HG-D and R4HG-4I-D) hydrogels. The morphology of R4HG-D and R4HG-4I-D was examined by optical microscopy and SEM, while UV–vis analyses were carried out to obtain the drug loading (DL%) and the encapsulation efficiency (EE%) of R4HG-4I. Potentiometric titrations were performed to determine the equivalents of NH3+ in both R4HG and R4HG-4I. The swelling and water release profiles of both materials and related kinetics were assessed by equilibrium swelling rate and water loss studies, respectively, while their biodegradability over time was assessed by in vitro degradation experiments determining their mass loss. Rheological experiments established that both R4HG and R4HG-4I are shear-thinning Bingham pseudoplastic fluids with low yield stress, thus assuring easy spreadability in a future topical application. Release studies evidenced a sustained and quantitative release of 4I governed mainly by diffusion. Upon favorable results from further experiments in a more realistic 3D model of melanoma, R4HG-4I could represent a starting point to develop new topical therapeutic options to adjuvate the treatments of melanoma cells also when resistant to currently available drugs. Full article
(This article belongs to the Special Issue Emerging Strategies to Improve the Design and Manufacturing of Biocompatible Therapeutic Materials, 2nd Edition)
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