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AL

alendronate sodium (Fosamax 70 / Alendil 70 / Endrox)

✓ Approved

Merck & Co. · Small Molecule · Small Molecule

What is alendronate sodium?

alendronate sodium is a small molecule developed by Merck & Co.. It is approved for therapeutic indications via oral (po).

Drug Profile

Brand NamesFosamax 70, Alendil 70, Endrox
CompanyMerck & Co.
Drug ClassSmall Molecule
RouteOral (PO)
StatusApproved

Therapeutic Indications

alendronate sodium is developed for 1 unique indication across 1 therapeutic area.

Therapeutic AreaConditionPhase
Musculoskeletal and connective tissue disordersOsteoporosis✓ Approved

Related Research Articles

PubMedTherapeutic advances in musculoskeletal disease2026-07-24

Longitudinal osteoporosis therapy: treat-to-target and sequential strategies-a narrative review.

Tskhakaia Irakli I, Danila Maria I MI

Osteoporosis is a chronic skeletal disorder in which reduced bone strength confers sustained fracture risk, often necessitating long-term pharmacotherapy with a multi-phase approach rather than a single "one and done" drug choice. Contemporary guidelines increasingly advocate a treat-to-target (TTT), goal-directed approach: clinicians define an explicit target, most often a total hip T-score threshold that corresponds to a lower fracture risk than baseline; select initial therapy according to baseline risk; and reassess and adjust treatment intensity until that target is achieved and maintained. Within this framework, sequential strategies are central. Anabolic-first sequences (e.g., abaloparatide or teriparatide followed by alendronate, or romosozumab followed by alendronate or denosumab) consistently produce larger and more durable gains in bone mineral density and fracture risk reduction in very-high-risk patients than antiresorptive monotherapy. Transitions from long-term bisphosphonates to teriparatide are complicated by transient increased remodeling and modest hip BMD responses, whereas switching to romosozumab yields more robust bone mineral density (BMD) gains at the hip. Notably, denosumab discontinuation demands structured bisphosphonate "exit" therapy to avoid rebound bone loss and multiple vertebral fractures. Across all pathways, rare but serious adverse events (e.g., atypical femoral fractures, medication-related osteonecrosis of the jaw, cardiovascular events), patient adherence and persistence, and insurance coverage constraints strongly shape the feasibility and desirability of specific regimens. This narrative review synthesizes mechanistic and clinical evidence underlying TTT osteoporosis care, summarizes the evidence base for sequential osteoporosis pharmacotherapy, and proposes practical strategies to help clinicians choose, transition, and discontinue therapies while preserving skeletal gains and minimizing harm over decades of longitudinal osteoporosis care.

PubMedJournal of thrombosis and thrombolysis2026-07-24

Localized antithrombotic but minimal systemic coagulation effects of sodium bicarbonate in mechanical circulatory support.

McKellar Kaitlyn R KR, Arviso Nizhoni N, Outridge Christine E CE, Tigrero Michelle M et al.

Sodium bicarbonate has recently emerged as an alternative additive to purge flow in microaxial blood pumps, offering local antithrombotic effects. However, the systemic effects of additive bicarbonate on coagulation remain incompletely defined. Here, we examined the effect of sodium bicarbonate at varying concentrations (10- 2-10- 5M) on select coagulation parameters to define systemic versus local effects. Fresh human whole blood from healthy adults (N ≥ 4 per assay) was incubated with sodium bicarbonate over a range of concentrations (10- 5-10- 2M). Coagulation and thrombus formation was assessed via whole blood clotting time (WBCT), activated partial thromboplastin time (aPTT), prothrombin time (PT), rotational thromboelastometry (ROTEM) and total thrombus analysis (T-TAS). Sodium bicarbonate at concentrations 10- 3M or less, did not induce significant changes in WBCT, aPTT, PT, ROTEM clot stiffness, or thrombus formation. Notably, at higher bicarbonate concentrations (10- 2M) WBCT was delayed (2.5 ± 0.5 min; p = 0.02), aPTT showed a moderate delay (3.9 ± 2.2 s; p > 0.05), ROTEM revealed increased clot stiffness at 10 min (1.7 ± 0.3 mm; p = 0.004) with high concentrations (10- 2 M) and a moderate decrease in thrombus formation (33.5 ± 21.9Kpa∙min; p > 0.05). Sodium bicarbonate, at concentrations encountered during intravenous (IV) use or expected systemic dilution during Impella purge use, was not associated with statistically significant alterations in global coagulation or platelet thrombosis in this in vitro study. Supraphysiologic levels, consistent with via intra-device purge flow in the device microenvironment, produced measurable but mild changes to clotting time and stiffness. These findings underscore the safety and lack of confounding effect of low dose systemic bicarbonate on systemic coagulation, while supporting mechanisms of local device-based antithrombotic efficacy.

PubMedCarbohydrate polymers2026-07-24

A thorough synthesis and structural investigation of a new generation of halide inclusion complexes of sodium β-cyclodextrin-based metal organic frameworks.

Ez-Zoubi Amine A, Benmansour Samia S, Gómez-García Carlos J CJ, Farah Abdellah A et al.

We report, for the first time, the ability of sodium(I)-based β-CD-MOFs (Na-β-CD-MOFs) to form Inclusion complexes (IC) with all the common halides, abbreviated as NaX-β-CD (X = F-, Cl-, Br- or I-). NaX-β-CD were obtained by a straightforward reaction of β-CD in an aqueous medium containing sodium halide (NaX) in an equimolar ratio, followed by the addition of a small amount of ethanol to induce crystallisation at room temperature. This series has been thoroughly characterised using single-crystal and powder XRD analysis, SEM-EDX, FTIR and 1H NMR spectroscopies. Morphological analysis via SEM revealed the coexistence of porous and block-shaped crystals, while EDX spectra confirmed the presence of sodium cations and the corresponding halide anions. Single-crystal X-ray diffraction analysis of NaF-β-CD shows the formation of a cationic sodium(I)-β-cyclodextrin double chain coordination polymer, whereas the F- anions are encapsulated within the bowl-like internal cavities of β-CD through a strong hydrogen bonding interaction, forming a host-guest (H2O)nF ⊂ β-CD IC. Powder XRD analysis of NaX-β-CD revealed that all these β-CD-MOF-based ICs are isostructural, regardless of the size of the halide anion (X = F-, Cl-, Br- or I-). FTIR and 1H NMR spectra confirmed the preservation of the β-CD skeleton, with minor changes in peak intensity and position.

PubMedCarbohydrate polymers2026-07-24

An AI-informed framework for flavor design: How κ-carrageenan sculpts low-sodium myofibrillar protein architecture for aldehyde capture and bitterness masking.

Huang Rong R, Fang Yapeng Y, Yin Hao H, Zhong Yu Y et al.

Designing healthy, palatable foods is a grand challenge in materials science, particularly in quest for low-sodium products where flavor is often compromised. The central problem is not merely replacing NaCl, but re-engineering the food matrix itself to manage off-flavors and retain desirable aromas. Here, an AI-informed framework demonstrates how the biopolymer κ-Carrageenan (KC) can sculpt the myofibrillar protein (MP) architecture for enhanced aldehyde capture and bitterness masking in low-sodium systems. Results showed KC acts as a molecular scaffold, transforming the protein from a rigid state into a porous, aggregated network. This remodeling significantly boosted binding for key flavor aldehydes (3-methylbutanal < pentanal < hexanal < heptanal). KC modulated MP-heptanal interactions primarily involved hydrogen bonding, whereas other aldehydes interacted mainly via hydrophobic forces. Concurrently, KC's sulfate groups sequestered K+, masking bitterness while enhancing saltiness and umami. To decipher this interplay, an interpretable machine learning model (R2 > 0.9) quantitatively linked conformational changes to flavor. SHAP analysis then revealed aldehyde concentration, protein solubility, and thiol group availability as the most critical features governing aldehyde absorption and bitterness perception. This work pioneers a structure-driven, Al-based strategy for flavor design, offering a new paradigm for the rational formulation of next-generation healthy foods.

PubMedCarbohydrate polymers2026-07-24

Carboxy group-rich cellulose fibers and nanofibrils from wood cellulose by aqueous catalytic oxidation with sodium dichloroisocyanurate.

Hou Runqing R, Chitbanyong Korawit K, Arnandan Pavitra Thevi PT, Shibata Izumi I et al.

Aqueous catalytic oxidation with 2,2,6,6-tetramethylpiperidine-1-oxyl radical and sodium dichloroisocyanurate (NaDCC) at pH 9 and ~23 °C is an environmentally adaptable system for the position-selective oxidation of the C6-OH groups of crystalline wood cellulose microfibril surfaces to sodium C6-carboxylate groups without significant depolymerization or side reactions. Carboxy contents of the water-insoluble oxidized products increased from 0.02 to 0.06 mmol/g up to 1.1-1.5 mmol/g (i.e., increases of 18-75 times) by oxidation. Nevertheless, the fibrous morphologies and molar masses of the oxidized products were nearly the same as those of the original wood cellulose fibers. The water-insoluble oxidized products were then converted into nearly individualized cellulose nanofibrils with homogeneous widths and lengths of >1 μm via mechanical fibrillation in water. Consequently, the NaBr/NaClO-free catalytic oxidation system with NaDCC for wood cellulose fibers can be regarded as a green chemical process for the preparation of carboxy group-rich cellulose fibers and nanofibrils. Crystalline wood-cellulose microfibril models were proposed based on the homogeneous chemical and solid-state structures of the oxidized products. The abundant carboxy groups in the oxidized cellulose fibers/nanofibrils are possibly used as scaffolds to introduce various cationic compounds for further functionalization by a simple ion-exchange treatment in water.

PubMedACS omega2026-07-24

In Situ Growth of Vertically Aligned Gold Nanoparticles within Functionalized Polyvinylidene Fluoride Nanochannels for Optical Property Tuning.

Aubrit Florian F, Sigallon Marie M, Oral Ozlem O, Medjoubi Kadda K et al.

A solid synthetic pathway for the localized formation of vertically aligned and well-distributed individual gold nanoparticles (AuNPs) in transparent ion-track-etched polyvinylidene fluoride membranes is herein reported. After a successful preconcentration of the Au-(III) precursor within the functionalized cylindrical nanochannels of these membranes, i.e., ion-track-etched radiografted with poly-(4-vinylpyridine) (P4VP), a Au-(IIII)-to-Au(0) chemical reduction was performed to in situ grow AuNPs inside the nanopores. Four classical reducing agents [ascorbic acid, hydroquinone, sodium citrate, and sodium borohydride (NaBH4)] were studied, which led, at first glance, to similar composites. The reducing power of each reducing agent has been shown to affect the AuNP nucleation and growth processes. At room temperature, the reduction led to the synthesis of well-dispersed AuNPs along the whole pore length, with the exception of sodium citrate, which was found to be too weak to reduce efficiently the gold precursor. When energy was provided to the system by operating the reaction at 70 °C, the reduction was boosted and the synthesis with sodium citrate gave similar results to those obtained with the other reducing agents at 20 °C, i.e., well-distributed AuNPs of around 30 nm of mean size. Increasing the number of reduction cycles resulted in an increase in AuNP size and, in the case of hydroquinone, in the elongation of the gold nanocrystals. This phenomenon was attributed to template-assisted AuNP growth in the nanopores. Despite the low amount of gold in the material (less than 0.2 %), the alignment of individual AuNPs all along the high aspect ratio nanopores (50:10,000) had a significant effect on the optical properties of the whole material, with the appearance of plasmonic properties for the nanocomposite membranes (λplasmon around 530 nm) and a further decrease of the effective refractive index of the nanoporous membranes.

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