Publications by authors named "A I Fabregues Olea"

Article Synopsis
  • A scoping review conducted between April and May 2022 mapped digital health initiatives aimed at elderly individuals and their caregivers, using established methodologies and various databases.
  • The review analyzed 421 documents, most of which were published from 2013 to 2022, highlighting a trend towards home-based applications primarily tested in high-income countries, with common devices being telephones and computers.
  • Findings indicate a growing role of technology for health monitoring, prevention, and treatment, yet emphasize the need for more research focused on middle- and low-income countries and on the effectiveness of these digital health interventions.
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In this work, a novel chitosan-based polyelectrolyte complex (PEC) was prepared using chitosan as the cationic polyelectrolyte, while a potassium salt of poly(maleic anhydride-alt-tetradecene) (PMA-14) served as the anionic counterpart. These PECs were used for the encapsulation of two nitroeugenol derivatives: 4-allyl-2-methoxy-6-nitrophenol () and 2-allyl-6-nitrophenol (). The results confirm complex formation and efficient encapsulation of active compounds.

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This study examined the association between healthcare access and quality of life (QOL) among senior citizens in Pampanga, Philippines. We conducted a cross-sectional study among 410 community-dwelling senior citizens aged 60 and above. Using validated scales, we assessed both healthcare access and QOL.

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Much work has been dedicated to the quest to determine the structure-activity relationship in synthetic brassinosteroid (BR) analogs. Recently, it has been reported that analogs with phenyl or benzoate groups in the alkyl chain present activities comparable to those shown by natural BRs, depending on the nature of the substituent in the aromatic ring. However, as it is well known that the activity depends on the structure of the whole molecule, in this work, we have synthesized a series of compounds with the same substituted benzoate in the alkyl chain and a hydroxyl group at C3.

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Brassinosteroids (BRs) are an important group of polyhydroxylated naturally occurring steroidal phytohormones found in the plant kingdom in extremely low amounts. Due to the low concentrations in which these compounds are found, much effort has been dedicated to synthesizing these compounds or their structural analogs using natural and abundant sterols. In this work, we report the synthesis of new brassinosteroid analogs obtained from hyodeoxycholic acid, with a 3,6 dioxo function, 24-Nor-22()-hydroxy side chain and -substituted benzoate function at C-23.

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