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hydroquinone (Tanit)

✓ Approved

Vinas · Small Molecule · Small Molecule

What is hydroquinone?

hydroquinone is a small molecule developed by Vinas. It is approved for therapeutic indications.

Drug Profile

Brand NamesTanit
CompanyVinas
Drug ClassSmall Molecule
StatusApproved

Therapeutic Indications

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

Therapeutic AreaConditionPhase
Skin and subcutaneous tissue disordersSkin hyperpigmentation✓ Approved

Related Research Articles

PubMedJournal of Nepal Health Research Council2026-08-25

Effectiveness of Intranasal Dexmedetomidine for Sedation in Children.

Sharma Mona M, Gongal Swagat S, Yadav Bijesh B, Shrestha Ashish Lal AL et al.

Preoperative sedation in children is necessary as it is a common source of distress, potentially leading to difficult induction. Intranasal dexmedetomidine bypasses hepatic metabolism and has good availability. It is non invasive, easy with minimal respiratory depression. This study aimed to observe safety, efficacy, sedation level and parental separation score following a fixed dose of 1.5 mcg/kg Methods: A cross sectional study design was conducted among 43 children posted for elective surgeries. After informed consent and assent were obtained, intranasal DEX 1.5mcg/kg was administered. Satisfactory sedation was defined as a Modified Observer's Assessment of Alertness/Sedation (MOAA/S) score of ? 3, and satisfactory parental separation as a score of ? 2 on a 4-point scale. Physiological parameters (HR, RR, SPO2 were monitored for 30 minutes. Statistical analysis involved the use of SAS version 9.4. Satisfactory sedation ? 3 was achieved in 93.0% of subjects by 30 minutes (95% CI: 80.9%-98.5%). Similarly, satisfactory parent-child separation ? 2 score was achieved in 93.0% of subjects. Mean heart rate progressively decreased from 107.12±14.20 at baseline to 85.47 ± 7.29 beats per minute at 30 minutes, which was well tolerated. Intranasal DEX at a dose of 1.5 mcg/kg is safe and effective premedication for paediatric patients, which results in successful sedation with tolerated changes in vitals.

PubMedJournal of medical virology2026-08-25

Enhanced Immunogenicity and Cross-Neutralizing Activity of a Trivalent Adenoviral Vector-Based SARS-CoV-2 Vaccine in Mice.

Li Jianhua J, Song Wanchen W, Li Jiaxuan J, Peng Ruofan R et al.

The emergence of diverse SARS-CoV-2 Omicron subvariants has reduced the efficacy of existing vaccines, highlighting the need for multivalent vaccines with broader neutralizing capacity. We developed a trivalent adenoviral vector-based vaccine (Ad5-CoV19-prototype/Delta/BF.7) encoding the spike proteins of the ancestral strain, Delta variant, and Omicron BF.7 strain, and evaluated its immunogenicity in BALB/c mice. Four- to 6-week-old female BALB/c mice were intramuscularly immunized with 10 µg of monovalent or trivalent vaccines using single-dose or two-dose (2-week interval) regimens. Neutralizing antibody (nAb) titers against the ancestral strain, Omicron BA.5, and XBB.1.5, as well as IFN-γ+ T-cell responses, were measured. The trivalent vaccine elicited significantly higher nAb titers against the ancestral strain (GMT 2183.6 at week 8) and Omicron subvariants (BA.5: GMT 680.0; XBB.1.5: GMT 161.3) after two doses compared to monovalent vaccines. Two doses also enhanced IFN-γ+ CD8+ T-cell responses (p < 0.0001). These results demonstrate that the trivalent vaccine induces enhanced immunogenicity and cross-neutralizing activity, including improved cross-neutralizing antibody titers and IFN-γ+ T-cell responses against multiple SARS-CoV-2 variants compared to monovalent formulations. These findings suggest potential for broader immune coverage against antigenically drifted variants, although protective efficacy remains to be confirmed in viral challenge models and further clinical evaluation.

PubMedPaediatric anaesthesia2026-08-25

Ultrasound-Based Assessment of Gastric Fluid Volume in the Pediatric Population Undergoing Elective Surgery: A Prospective, Randomized, Double-Blind Comparison of Carbohydrate-Rich Clear Fluid Versus Water at One- and Two-Hour Fasting Intervals.

Parameswari Aruna A, Som Amrit Kumar AK, Manivannan Kishore K, Paul Anisha Pauline AP et al.

Preoperative fasting guidelines have evolved from the traditional "nil per os after midnight" rule toward more liberal regimens. The European Society of Anaesthesiology and Intensive Care (ESAIC) and the Association of Pediatric Anesthetists of Great Britain and Ireland (APAGBI) now recommend a one-hour clear fluid fast for children, yet objective evidence quantifying the gastric fluid volume (GFV) resulting from carbohydrate-rich clear fluids at this abbreviated interval remains limited. To evaluate the effect of one- versus two-hour fasting following the ingestion of 3 mL/kg of a carbohydrate-rich clear fluid or plain water on GFV, as assessed by point-of-care gastric ultrasound (POCUS), in healthy children undergoing elective surgery. In this prospective, randomized, double-blind, parallel-group trial (CTRI/2024/01/061823) conducted at a tertiary referral centre from February 2024 to March 2025, 140 ASA I-II children aged 1-12 years undergoing elective non-gastrointestinal surgery were randomized to one of four groups: (A) 10% glucose solution (Glucon-D), 1-h fast; (B) 10% glucose solution, 2-h fast; (C) plain water, 1-h fast; (D) plain water, 2-h fast. All children received 3 mL/kg of the assigned fluid and fasted for the designated interval before POCUS assessment. The primary outcome was GFV in the right lateral position (RLP), calculated using the Spencer formula. Secondary outcomes included GFV distribution across three risk thresholds (0.8, 1.25, and 1.5 mL/kg), antral cross-sectional area (CSA) in supine and RLP, qualitative Perlas antral grading (Grades 0-2), prevalence of pulmonary aspiration, and Visual Analogue Scale (VAS) comfort scoring. All 140 enrolled children completed the study. Mean GFV in RLP was highest in Group A (0.947 ± 0.225 mL/kg), followed by Group C (0.825 ± 0.179 mL/kg), Group B (0.340 ± 0.317 mL/kg), and Group D (0.268 ± 0.322 mL/kg) (one-way ANOVA, p < 0.001). No participant in any group exceeded a GFV of 1.5 mL/kg. In Group A, 57.1% of children had GFV between 0.9-1.25 mL/kg; 91.4% of Group B and 100% of Group D had GFV ≤ 0.8 mL/kg. Perlas Grade 2 was observed in 31.4% of Group A and 8.6% of Group C; none in the two-hour groups. VAS comfort scores were significantly higher in Group A (8.31 ± 0.63) compared to Group D (6.66 ± 0.97) (p < 0.001). No episodes of pulmonary aspiration occurred. Consumption of 3 mL/kg of a carbohydrate-rich clear fluid 1 h before anesthesia induction produces higher but clinically safe GFV (none exceeding 1.5 mL/kg) and superior patient comfort compared to conventional two-hour fasting. These findings provide prospective, quantitative support for the implementation of one-hour clear fluid fasting protocols in healthy pediatric patients undergoing elective surgery. The trial was registered prospectively with the Clinical Trials Registry (India), CTRI/2024/01/061823.

PubMedBiomedical chromatography : BMC2026-08-25

Optimization of the Extraction of Total Alkaloids From Lotus Leaves by Acidic Ethanol and Its Purification by Macroporous Resins.

Zhang Xueping X, Wu Yuchen Y, Li Chenglin C, Feng Yichao Y et al.

This acidic ethanol extraction method was adopted to extract total alkaloids from lotus leaves. Single-factor experiments combined with response surface methodology (RSM) were employed to optimite extraction conditions. The optimal extraction parameters were determined as follows: 55 °C, 77% ethanol, 0.66% hydrochloric acid, under which the extraction yield of total alkaloids reached 4.14%. D101 macroporous resin was selected for the purification of crude alkaloid extracts. The resin exhibited an adsorption capacity of 8.60 mg/g and a desorption rate of 43.39%. The optimized purification conditions were as follows: 4 mg/mL sample solution, 50% ethanol eluent, 1.5 BV/h flow rate, 30 mL loading/100 mL elution volume. After purification, total alkaloid purity reached 89.31 ± 1.33%. Adsorption obeyed pseudo-second-order kinetics and Temkin isotherm, being spontaneous and endothermic. This provides improved methods for isolating bioactive alkaloids from lotus leaf.

PubMedJournal of perinatology : official journal of the California Perinatal Association2026-08-25

Consensus-based eligibility criteria and component definitions for neonatal and infant enhanced recovery pathway: a multidisciplinary delphi study.

Borst Johanna M JM, Raval Mehul V MV, Perez Mallory N MN, Falciglia Gustave H GH et al.

The 2020 Enhanced Recovery After Surgery (ERAS®) guidelines for neonatal intestinal surgery have not been widely implemented due to unclear eligibility criteria and poorly defined components. We sought to establish consensus-based eligibility criteria and definitions for a revised enhanced recovery pathway (ERP). We conducted two modified Delphi processes to establish eligibility criteria and define the components by engaging stakeholders including surgeons, anesthesiologists, neonatologists, nurses, dietitians, quality improvement specialists, and parents/caregivers at six pediatric hospitals. Eligibility criteria were established through two survey rounds; components were defined through two survey rounds and one focus group. Forty-five stakeholders participated (82% response). Consensus supported inclusion of infants born ≥32 weeks' gestation or ≥1.5 kg undergoing elective/semi-urgent gastrointestinal surgery and defined 19 components, with 10 initially accepted and 9 revised. The consensus-based Delphi process established eligibility and defined the components to facilitate implementation and adoption of an ERP for neonates and infants undergoing gastrointestinal surgery.

PubMedSexual abuse : a journal of research and treatment2026-08-25

Does Failure to Register Matter? A Retrospective Comparison of Men on Probation for Sexually-Related Offenses.

Alarid Leanne Fiftal LF, Matz Adam K AK

This study examined the extent to which men sentenced to probation for Violation of Sex Offender Registration and Notification Act (registration violations) differed from individuals sentenced directly to probation for a sex offense in a large urban county. All individuals in the study were revoked from probation over a three-year period. Variables of interest include actions that led to probation revocation, court-ordered condition violations that preceded revocation, court-ordered treatment requirements, criminal history, prior victimization, and other demographic characteristics. We found that the registration violation group was more likely to violate several conditions of probation, less likely to possess steady employment, and more likely to possess a history of prior charges including registration violations, drugs, theft and burglary, as compared to individuals directly sentenced to probation for a sex offense. Individuals in the registration violations group were also revoked with greater immediacy, within about 1.5 months on average compared to 3 months for individuals directly sentenced to probation. Probation officers may benefit from recognizing registration violation behaviors as distinctly different so that responses and strategies may be tailored to the greater likelihood of substance dependency, general criminality, and less cooperative tendencies.

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