4.8 Article

Coordination Compounds As Multi-Delivery Systems for Osteoporosis

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 30, 页码 35469-35483

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c09121

关键词

osteoporosis; bisphosphonates; coordination compounds; controlled release; toxicological safety

资金

  1. University of Aveiro [UIDB/50006/2020, UIDB/50011/2020, UIDP/50011/2020, UIDB/00081/2020]
  2. Foundation for Science and Technology/MCTES [UIDB/50006/2020, UIDB/50011/2020, UIDP/50011/2020, UIDB/00081/2020]
  3. FEDER, within the PT2020 Partnership Agreement
  4. FEDER through COMPETE 2020 [022161]
  5. FEDER through POCI [022161]
  6. FEDER through PORL [022161]
  7. FCT through PIDDAC [022161]
  8. FCT/MCTES [UIDB/04378/2020]

向作者/读者索取更多资源

The study presents an all-in-one combination therapy for osteoporosis by incorporating four antiosteoporotic components into coordination complexes. These compounds have the potential to effectively manage chronic bone diseases, warranting further research on their therapeutic properties.
Osteoporosis therapies leveraging bisphosphonates and mineral components (e.g., magnesium, calcium, and strontium) have been raising attention because of their potential for managing this ever-growing disease. The administration of multicomponent therapeutics (combined therapy) in elderly patients is complex and suffers from low patient adherence. Herein, we report an all-in-one combination of four antiosteoporotic components into a new family of coordination complexes: [M-2(H(4)alen)(4)(H2O)(2)]center dot 1.5H(2)O [where M2+ = Mg2+ (1), (Mg0.535Ca0.465)(2+) (2) and (Mg0.505Ca0.450Sr0.045)(2+) (3)]. These solid-state complexes were prepared, for the first time, through microwave-assisted synthesis. It is demonstrated that the compounds are capable of releasing their antiosteoporotic components, both in conditions that mimic the path along the gastrointestinal tract and in long periods under physiological conditions (pH similar to 7.4). More importantly, when administered in low concentrations, the compounds did not elicit a cytotoxic effect toward liver, kidney, and osteoblast-like cell lines. Besides, it is important to highlight the unique coordination complex with four bone therapeutic components, [(Mg0.505Ca0.450Sr0.045)(2)(H(4)alen)(4)(H2O)(2)]center dot 1.5H(2)O (3), which significantly promoted osteoblast metabolic activity up to ca. 1.4-fold versus the control group. These findings bring this type of compounds one-step closer to be considered as an all-in-one and more effective treatment for managing chronic bone diseases, prompting further research on their therapeutic properties.

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