In recent years, alternative pulpal therapies targeting dentinogenesis signaling pathways using different peptides have been investigated. The aim of this study was to verify the effectiveness of poly(aspartic acid), pAsp, in dentin regeneration using an animal model. Methods: Mechanical pulp exposure was performed in the upper molars of 56 Wistar rats, randomly divided as follows (n = 14): control (no treatment); MTA group—pulp capping with mineral trioxide aggregate (MTA Angelus); pAsp group—application of 20 μL of pAsp solution (25 mg·mL⁻¹); MTA+pAsp group—application of MTA mixed with pAsp (5:1 by mass). Animals were euthanized after 7 or 21 days. Histological sections were submitted to hematoxylin-eosin and Brown and Brenn staining and immunohistochemical analysis for osteopontin (OPN) and dentin matrix protein 1 (DMP 1). Results: At 7 days, an acute inflammatory infiltrate and the presence of disorganized mineralized tissue were observed in all groups. At 21 days, the quality and thickness of the reparative dentin in treated groups were superior to the control, and bacterial contamination was observed in two MTA-pAsp specimens. While all treated groups showed intense immunostaining for OPN at 21 days, only the pAsp group expressed DMP 1, indicating the presence of fully differentiated odontoblast-like cells. Conclusion: Poly(aspartic) acid promoted dentin regeneration in rat molars in the absence of an additional calcium source and may be an alternative to MTA as a pulp-capping agent.

O processo de envelhecimento facial tem causas naturais e multifatoriais, ocorrido por fatores intrínsecos (envelhecimento celular natural) e extrínsecos (radiação solar, por exemplo), os quais, geram mudanças e podem levar ao desconforto com a aparência.O objetivo neste estudo foi observar as indicações de tratamentos para o fotoenvelhecimento com diferentes ácidos a fim de minimizar rugas, manchas, cicatrizes, acne, o aspecto de pele desidratada, entre outros. Trata-se de um estudo de revisão de literatura, realizado entre os anos de 2024 e 2025. Foram consultados diversos periódicos da área, assim como as bases de dados Pubmed, Scielo, Lilacs e Medline, mostrando as indicações, os benefícios, recomendações, contra-indicações, bem como as complicações do uso de cada ácido. As principais variáveis encontradas nos tratamentos químicos foram: o tipo de ácido utilizado, a concentração, o tempo de aplicação e o tipo de dano causado à pele do rosto. De acordo com o dano encontrado na pele, foi aplicado certo tipo de produto químico, cujo princípio ativo deveria ser um tipo de ácido, selecionado de acordo com a profundidade e lesão a qual se deseja atuar, desde manchas superficiais, às rugas ou cicatrizes, em camadas mais profundas. A literatura aponta que o procedimento de quimioabrasão, também chamado de peeling químico é altamente eficaz no tratamento de lesões e danos causados pelo processo de fotoenvelhecimento, devendo, no entanto, ser utilizado por profissionais com habilidade e experiência, assim como devem ser adotados protocolos reconhecidamente seguros e eficazes.

Dentin–pulp regeneration has shifted from passive repair toward biologically guided strategies that preserve pulp vitality and actively regulate the healing microenvironment. This narrative review critically discusses biomaterial-driven approaches for dentin tissue engineering and their potential application in vital pulp therapy. Relevant literature was narratively selected according to thematic relevance, methodological contribution, and translational significance, without a formal systematic-review protocol or quantitative study-selection process; no fixed publication-date restriction was imposed, and both seminal and recent studies were considered. The evidence indicates that naturally derived polymeric scaffolds, nanofibrous membranes, injectable and photocrosslinkable hydrogels, microsphere-based delivery systems, and three-dimensional printed scaffolds can combine structural support with mineral signaling, immunomodulation, endogenous cell recruitment, angiogenesis, odontoblast-like differentiation, and controlled bioactive-agent delivery. Cell-homing and multifunctional platforms are particularly relevant for clinical translation because they may support pulp-preserving therapies without exogenous cell transplantation and may be integrated with familiar restorative procedures. However, most evidence remains preclinical and heterogeneous. Future translation requires standardized dentin-based, inflammatory, microbial, and orthotopic models, together with validation of handling, curing, sealing, degradation, safety, and long-term pulp vitality under clinically relevant conditions.

The contemporary management of dentin injuries has progressively shifted from approaches based solely on reparative mineralized barrier formation toward biologically guided strategies that preserve pulp vitality and promote endogenous regeneration. This paradigm change has driven the development of bioactive biomaterials capable of modulating the dentin–pulp microenvironment rather than serving exclusively as passive sealing materials. This review critically discusses recent advances in biomaterial-based approaches for dentin tissue engineering, emphasizing naturally derived polymeric scaffolds, nanofibrous membranes, injectable hydrogels, microsphere-based delivery systems, and three-dimensional (3D)-printed scaffolds. The biological mechanisms by which these platforms regulate inflammation, recruit endogenous progenitor cells, stimulate angiogenesis, direct odontoblast-like differentiation, and promote extracellular matrix deposition are highlighted. Particular attention is given to the sequential development of mineral-functionalized nanofibrous scaffolds, from the selection of calcium hydroxide and nano-hydroxyapatite as bioactive phases to the incorporation of fibronectin and, subsequently, the flavonoids quercetin and hesperetin to combine odontogenic signaling with immunomodulation. Emerging concepts, including immunoinstructive biomaterials, cell-homing strategies, smart hydrogels, and biofabrication technologies, are discussed in the context of their translational potential for vital pulp therapy. Rather than focusing exclusively on recreating the native tubular architecture of dentin, current regenerative strategies increasingly seek to restore pulp homeostasis and establish biological conditions that enable predictable reparative dentinogenesis. Collectively, these advances position biomaterials as active regulators of tissue regeneration and provide a framework for next-generation therapies aimed at preserving pulp vitality and improving the long-term outcomes of dentin regeneration.