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1.
Pak J Pharm Sci ; 36(5(Special)): 1649-1656, 2023 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-38008963

RESUMEN

In terms of delivery systems for active compounds, orally disintegrating films are a great option. The initial stage in creating an oral disintegrating film is selecting a film-forming polymer. The basic polymers combination Microcrystalline Cellulose (MCC), which is co-processed with Carboxymethylcellulose Sodium (CMC) and hydroxypropylmethyl cellulose were used to create an oral disintegrating film that contains cholecalciferol (Vitamin D3), a fat-soluble vitamin that aids in the body's absorption of calcium and phosphorus. The goal of the current inquiry was to develop orally disintegrating films of vitamin D3 to improve patient comfort and compliance for pediatric or elderly patients due to its simplicity of administration. Films containing drugs and made of the appropriate plasticizer and chosen polymers demonstrated outstanding film forming and folding endurance. The dissolution test showed that Vitamin D3 has a rapid disintegration property, with the majority of it dissolving in the medium (pH 6.8) in less than two minutes after being inserted. To verify that the films were successfully formed, a variety of procedures including HPLC, FT-IR and microscopic studies were employed. When kept at 40oC with humidity of 75%, the film showed good stability for at least three months.


Asunto(s)
Colecalciferol , Polímeros , Humanos , Niño , Anciano , Espectroscopía Infrarroja por Transformada de Fourier , Solubilidad , Polímeros/química , Derivados de la Hipromelosa/química , Administración Oral
2.
Heliyon ; 10(4): e26494, 2024 Feb 29.
Artículo en Inglés | MEDLINE | ID: mdl-38420404

RESUMEN

This research presents the design and implementation of a chipless Radio Frequency Identification (RFID) multi-sensor tag on a flexible laminate. Along with the tag's primary function of data encoding for object identification purposes, the tag also incorporates moisture and temperature sensing functionalities within a compact size measuring a mere 15 × 16 mm2. The tag structure comprises of a total 29 resonators, with each resonator corresponding to one bit in the microwave response. The initial design utilized the bendable Rogers RT/duroid®5880 within a frequency band of 5.48-28.87 GHz. To conduct a comprehensive comparative analysis, the tag design is optimized for two distinct substrates including Kapton®HN and PET. The optimization process involves exploring the utilization of both silver nanoparticle-based ink and Aluminum as radiators. The sensing feature was incorporated by deploying a thin film of Kapton®HN over the longest slot of the tag which acts as a moisture sensor. Temperature sensing feature was achieved by combining Stanyl® polyamide, a temperature dependent polymer, with Rogers RT/duroid®5880 which served as a fused substrate. The tag showcases a high code density of 12.08 bits/cm2 enabling it to efficiently label 229 unique items. Its unique features include flexibility, miniaturized design, printability, cost-effectiveness and multi sensing property.

3.
J Pharm Pharmacol ; 2024 Sep 25.
Artículo en Inglés | MEDLINE | ID: mdl-39321327

RESUMEN

OBJECTIVES: This study investigates the dual role of ALKBH5, an eraser enzyme, in colorectal cancer (CRC), focusing on how N6-methyladenosine (m6A) mutations influence CRC development and progression. METHODS: We reviewed various studies that highlighted the role of ALKBH5 in colorectal cancer (CRC). This includes the impact of ALKBH5 on tumor cell behavior including immune system interactions, invasion, and proliferation in CRC. We also looked into how ALKBH5 acts as a tumor suppressor under different conditions analyzed clinical data to assess the impact of ALKBH5 expression on outcomes in colorectal cancer patients. KEY FINDINGS: In CRC, ALKBH5 plays a dual role. In certain situations, it inhibits the progression of the tumor, but in other circumstances, it promotes tumor growth and immunosuppression. The interaction with RABA5 plays a role in the development of CRC. Having elevated levels of ALKBH5 has been associated with unfavorable patient outcomes, such as reduced survival rates and more advanced cancer stages. Various factors, including tumor differentiation, TNM stages, and carcinoembryonic antigen (CEA) levels, be linked to ALKBH5 expression. CONCLUSIONS: ALKBH5 plays a complicated and situation-specific role in colorectal cancer (CRC). Targeting ALKBH5 could result in novel therapy options that balance its tumor-promoting and tumor-fighting properties in CRC. Further research into m6A alterations and ALKBH5 could enhance CRC treatment approaches and patient outcomes.

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