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nitroglycerin (Millisrol Tape)

✓ Approved

Nippon Kayaku Co.,Ltd. · Small Molecule · Small Molecule

What is nitroglycerin?

nitroglycerin is a small molecule developed by Nippon Kayaku Co.,Ltd.. It is approved for therapeutic indications via transdermal.

Drug Profile

Brand NamesMillisrol Tape
CompanyNippon Kayaku Co.,Ltd.
Drug ClassSmall Molecule
RouteTransdermal
StatusApproved

Therapeutic Indications

nitroglycerin is developed for 1 unique indication across 1 therapeutic area.

Therapeutic AreaConditionPhase
Cardiac disordersAngina pectoris✓ Approved

Related Research Articles

PubMedAdvances in radiation oncology2026-08-30

Systemic Copper Chelation Reduces Collagen Deposition and Preserves Secretory Function in Irradiated Mouse Salivary Glands.

Nam Kihoon K, Maslow Frank M FM, Santos Harim Tavares Dos HTD, Shanbhag Vinit C VC et al.

Radiation therapy (RT) for head and neck cancer commonly causes fibrosis of the salivary gland (SG) and loss of secretory function. We previously demonstrated that transdermal injection of the copper chelator tetrathiomolybdate into irradiated submandibular glands reduced the early deposition of fibrillar collagen and preserved their integrity and function. Although these studies identified copper metabolism as a novel therapeutic target to control RT-induced damage to the SG, local delivery of copper chelators in human SG presents clinical hurdles including specialized personnel and equipment needed for administration together with the discomfort felt by patients upon receiving this treatment. To overcome these issues, the current study investigated whether systemic administration of tetrathiomolybdate (TTM) via drinking water could similarly reduce collagen deposition and preserve secretory function. Mice received TTM in drinking water (0.1 mg/mL) beginning 7 days before and continuing through 7 days after a single 15-Gy dose of RT to the neck. Systemic TTM exposure and copper bioavailability were assessed by measuring molybdenum and copper levels and serum ceruloplasmin activity. RT-induced SG injury was evaluated by collagen deposition, histopathology, epithelial integrity, and stimulated saliva secretion. Systemically administered TTM reached the submandibular gland and reversibly reduced copper bioavailability, as demonstrated by increased molybdenum levels, reduced copper-to-molybdenum ratios, and suppression of serum ceruloplasmin activity. Moreover, TTM treatment attenuated RT-induced collagen deposition and epithelial damage and promoted recovery of ZO-1 expression. Finally, at 30 days after RT, stimulated saliva flow was significantly higher in TTM-treated irradiated mice than in irradiated mice receiving regular water. Systemic TTM administration reduces copper bioavailability, attenuates RT-induced collagen deposition and epithelial injury, and preserves SG secretory function. These findings support systemic copper chelation as a less invasive alternative to local TTM delivery for limiting RT-induced SG damage.

PubMedHeart rhythm O22026-08-29

Efficacy and safety of pulsed field ablation for cavotricuspid isthmus-dependent atrial flutter: A meta-analysis based on real-world evidence.

Liu Lei L, Chen Aiyue A, Liu Linqi L, Maimaitijiang Pakezhati P et al.

Pulsed field ablation (PFA) is effective for atrial fibrillation, but its real-world performance for cavotricuspid isthmus (CTI)-dependent atrial flutter remains inadequately defined. The purpose of this study was to systematically evaluate the efficacy and safety of PFA for CTI ablation using real-world evidence. A total of 9 observational studies (656 patients) published up to January 2026 were analyzed using a random-effects model. Pooled analysis revealed a short-term bidirectional CTI block rate of 99.4% and a short-to-midterm recurrence rate of 2.14%. Mean CTI ablation time was highly efficient (8.86 minutes). Incidences of catastrophic complications and permanent atrioventricular block were 0%. The overall incidence of intraprocedural right coronary artery spasm was 2.0%. Prophylactic high-dose intravenous nitroglycerin (>1 mg) significantly reduced coronary spasm incidence compared with low-dose (≤1 mg) regimens (1% vs 8%; P = .0016). Sensitivity analyses confirmed spasm risk was independent of PFA catheter configuration (P = .9549). PFA is a rapid, safe, and highly effective modality for CTI ablation. The risk of transient coronary spasm may be mitigated with prophylactic high-dose nitroglycerin. These hypothesis-generating findings warrant further validation.

PubMedAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026-08-29

Integrated O2 and H2 Gas Therapy via Microneedle-Assisted Photocatalytic Water Splitting for Accelerating Diabetic Full-Thickness Skin Wound Healing.

Chen Zesheng Z, Yu Yanchao Y, Xiao Xingyuan X, Cheng Wenwen W et al.

Impaired wound healing in diabetes is closely associated with cellular ferroptosis. Microneedle-assisted gas therapy exerts molecular regulation of ferroptosis, representing a promising approach for accelerating diabetic wound healing. To date, O2 and H2 gas therapies have consistently been conducted independently and have never been integrated into a single system. Whether and how their synergy might be realized remains a defining challenge. Herein, we propose a concept of integrated O2 and H2 gas therapy, demonstrated by fabricating a gas-producing microneedle material. Platinum@MIL-101(Fe)-NH2@phosphotungstic acid (PMP) nanoparticles are synthesized as a visible light-driven photocatalyst for H2 and O2 co-evolution. The rational design of a spatially separated structure boosts their photocatalytic efficiency under physiological conditions. PMP nanoparticles are further incorporated with bilayer gelatin methacryloyl (GelMA)/PMP composite microneedles (denoted as GPM microneedles). The obtained GPM microneedles enable transdermal delivery of PMP nanoparticles for integrated O2 and H2 gas therapy, and demonstrate desirable biocompatibility and pro-regenerative effects. The mechanism of integrated O2 and H2 gas therapy has been identified as a TNFAIP3/hnRNPA1 ubiquitination/ferroptosis signaling axis, establishing for the first time a direct link to ferroptosis. In conclusion, this study yields a transformative concept and a ferroptosis-targeting microneedle material with well-defined molecular mechanism for diabetic wound management.

PubMedExploration (Beijing, China)2026-08-28

The Needle-Free Frontier: Redefining the Limits of Transdermal Insulin Delivery.

Chen Junge J, Liu Yuxuan Y, Xia Bozhang B, Essola Julien Milon JM et al.

Wei and colleagues reported a pH-responsive, charge-switchable polyzwitterionic polymer carrier that achieves non-invasive transdermal insulin delivery without external energy input. The approach leverages adaptive compatibility with the cutaneous microenvironment to shuttle functional macromolecules across intact skin and achieve definitive systemic therapeutic outcomes.

PubMedPharmaceutical development and technology2026-08-28

Innovative Hybrid Microneedle Patch for Co-delivery of Varenicline and Melatonin: Development, Characterization, and Potential for Smoking Cessation.

Shahriari Mohammad Hassan MH, Salmani Hossein H, Ghiass Mohammad Adel MA, Kamali Nader N et al.

This study aimed to develop a microneedle patch loaded with varenicline and melatonin to improve patient compliance and enhance transdermal delivery for smoking cessation. Smoking remains a major public health challenge. While varenicline is effective, oral administration can cause adverse effects, and vaccine-like approaches are limited by nicotine's small size. A painless, microneedle patch delivering varenicline together with melatonin could improve patient adherence and provide sustained delivery. Microneedle arrays were fabricated using a blend of polyvinyl alcohol (PVA) and polyvinylpyrrolidone (PVP), with Tween-80 added to enhance varenicline solubility. Comprehensive mechanical characterization, including nanoindentation, scratch testing, and atomic force microscopy, was performed. In vitro drug release and transdermal permeation studies were conducted, complemented by histological evaluation and fluorescence imaging. The microneedles exhibited high hardness, flexibility, and uniform surface topography, enabling effective skin penetration. In vitro studies showed cumulative transdermal permeation of 34.3% for varenicline and 41.6% for melatonin over 48 hours. The dual-drug-loaded microneedles demonstrated a sustained release profile. Histological analysis confirmed the creation of microchannels without damaging surrounding tissues. The combination of varenicline and melatonin in the microneedle shows promise in overcoming the limitations of current smoking cessation therapies, offering a patient-friendly and effective intervention. Future studies should include comparisons with commercial therapies and ex vivo dissolution studies (Q8).

PubMedACS omega2026-08-28

Modulation of Donepezil Release Through Hydrophobic Ion- Pairing with Oleic Acid in Liquid Crystalline Nanodispersions for Transdermal Delivery.

Pires da Silva Priscila P, Marques Victor Cavalcanti VC, Santiago Ramos Lorena Kelly LK, Filho José Dias de Souza JDS et al.

Precursor liquid crystals based on unsaturated monoglycerides, with or without oleic acid (OA), exhibited anisotropy characteristic of an inverse hexagonal phase. Donepezil-loaded liquid crystalline nanodispersions (LCNs) were produced by sonication and exhibited encapsulation efficiencies of 91.3-97.9%, with the OA-containing formulation (LCN-2) displaying a smaller particle size (183.0 ± 1.5 nm), lower polydispersity (0.183 ± 0.006), and improved colloidal stability over 90 days. NMR (1H NMR, 1D NOESY/ROESY and DOSY), molecular docking, and molecular dynamics simulations consistently demonstrated hydrophobic ion-pair formation between donepezil and oleic acid. These molecular interactions reduced drug mobility within the lipid domains, resulting in anomalous release behavior (n = 0.79), more sustained in vitro release, and an approximately 45% higher steady-state skin flux than the control donepezil solution. Overall, hydrophobic ion-pair formation with oleic acid represents an effective strategy to modulate drug release and enhance the transdermal performance of liquid crystalline nanodispersions for donepezil delivery.

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