Hydroxyapatite-Based Alendronate Coatings for Local Drug Delivery and Implant Osseointegration

Background/Objectives: Hydroxyapatite (HA) coatings offer an osteoconductive interface and a mineral reservoir for alendronate. Their pharmaceutical value depends on whether binding produces biologically available exposure without impairing healing. This review examines that relationship in HA–alendronate coatings on titanium. Methods: A structured critical narrative review used PubMed/MEDLINE, Scopus and Web of Science Core Collection, with reference-list screening. Screening identified 62 primary studies; contextual literature supported mechanistic and translational interpretation. Results: Adsorption, mineral incorporation, laser deposition and hybrid reservoirs produce different loading and release profiles. Cell and animal findings depend on formulation, dose, comparator and model. Mineral content, bone-to-implant contact and mechanical fixation provide complementary evidence and are not interchangeable outcomes. Human studies have mainly evaluated other bisphosphonates in fibrinogen coatings or alendronate applied as a gel around dental implants. Some reported less marginal bone loss, but improvements in implant stability were inconsistent. These results do not directly establish the efficacy of HA–alendronate coatings. Conclusions: Translation requires reproducible manufacture, measured active-drug availability, preserved physiological remodeling, durable coating adhesion and controlled trials for a defined implant indication. Strong mineral binding alone does not establish effective local therapy.

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Publication Details

Journal
Pharmaceutics
Published
2026-11-08
DOI
https://doi.org/10.3390/pharmaceutics18111447
Primary Topic
Bone Tissue Engineering Materials
Type
article
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article

Hydroxyapatite-Based Alendronate Coatings for Local Drug Delivery and Implant Osseointegration

Cristian Cosmin Arsenie, Bogdan Niculescu, Adina Maria Kamal, Diana-Maria Trașcă et al.
Pharmaceutics
Bone Tissue Engineering Materials
article

Hydroxyapatite-Based Alendronate Coatings for Local Drug Delivery and Implant Osseointegration

Cristian Cosmin Arsenie, Bogdan Niculescu, Adina Maria Kamal, Diana-Maria Trașcă, Renata Maria Văruț, Maria Stoica, Pirscoveanu Denisa Floriana Vasilica, Pluta Ion Dorin, Dirnu Rodica
article en

Abstract

Background/Objectives: Hydroxyapatite (HA) coatings offer an osteoconductive interface and a mineral reservoir for alendronate. Their pharmaceutical value depends on whether binding produces biologically available exposure without impairing healing. This review examines that relationship in HA–alendronate coatings on titanium. Methods: A structured critical narrative review used PubMed/MEDLINE, Scopus and Web of Science Core Collection, with reference-list screening. Screening identified 62 primary studies; contextual literature supported mechanistic and translational interpretation. Results: Adsorption, mineral incorporation, laser deposition and hybrid reservoirs produce different loading and release profiles. Cell and animal findings depend on formulation, dose, comparator and model. Mineral content, bone-to-implant contact and mechanical fixation provide complementary evidence and are not interchangeable outcomes. Human studies have mainly evaluated other bisphosphonates in fibrinogen coatings or alendronate applied as a gel around dental implants. Some reported less marginal bone loss, but improvements in implant stability were inconsistent. These results do not directly establish the efficacy of HA–alendronate coatings. Conclusions: Translation requires reproducible manufacture, measured active-drug availability, preserved physiological remodeling, durable coating adhesion and controlled trials for a defined implant indication. Strong mineral binding alone does not establish effective local therapy.

PharmaceuticsVol. 18(11)
University of Medicine and Pharmacy of Craiova (RO), Constantin Brâncuși University of Targu Jiu (RO), Spitalul Clinic Judetean de Urgentã Craiova (RO)
Bone Tissue Engineering Materials
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