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hyaluronidase (Amphadase)

✓ Approved

Amphastar Pharmaceuticals, Inc. · HYAL1

什么是 hyaluronidase?

hyaluronidase 是一种治疗药物,由Amphastar Pharmaceuticals, Inc.研发。该药已获批,用于治疗相关适应症,给药途径:Injectable (Others)、Subcutaneous Injection。

药物档案

商品名Amphadase
公司Amphastar Pharmaceuticals, Inc.
分子靶点HYAL1
给药途径Injectable (Others), Subcutaneous Injection
状态Approved

作用机制

分子靶点

hyaluronidase 作用于 1 个分子靶点:

HYAL1hyaluronidase 1 (LUCA1, MPS9)
需要更深入的分析?Noah AI 可解释复杂机制并与同类药物比较。

治疗适应症

hyaluronidase 针对 1 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Surgical and medical proceduresAdjuvant therapy✓ Approved

相关研究文献

PubMedProtoplasma2026-10-26

Morphological, anatomical, and phytochemical characterization of Sisymbrium altissimum L.: chemical composition, biological activities, and isolation of major constituents.

Tekman Enes E, Aydın Bilge B, Yuca Hafize H, Özbek Hilal H et al.

This study comprehensively evaluated the phytochemical composition and multidimensional biological activities of Sisymbrium altissimum L., a wild edible species belonging to the Brassicaceae family. Methanolic extracts obtained from aerial parts, flowers, fruits, and roots were successively fractionated using solvents of increasing polarity, and essential and fatty oils were characterized by GC-MS and GC-FID analyses. The essential oil composition showed marked organ-dependent variation, with methallyl cyanide dominating fruit (91.9%) and flower (75.9%) oils, while phenylethyl isothiocyanate (48.7%) was the major constituent in roots. Further phytochemical investigation of the biologically active root hexane extract led to the isolation of β-sitosterol, lauric acid, and β-sitosterol-3-O-glucoside. Biological activity assays revealed strong α-glucosidase inhibition, particularly in the root hexane extract (87.92%), exceeding the reference drug acarbose (68.49%), whereas α-amylase inhibition was moderate, with the root ethyl acetate fraction exhibiting the highest activity (40.84%). Cholinesterase inhibition assays demonstrated low to moderate acetylcholinesterase and butyrylcholinesterase inhibitory activities depending on the plant part and extract fraction. Hyaluronidase inhibition was notably high, reaching up to 98.70%, whereas moderate collagenase (27.56%) and elastase (23.98%) inhibition and low tyrosinase activity were observed. Antioxidant activity was prominent in ethyl acetate and n-butanol fractions, with ABTS radical scavenging values approaching those of standard antioxidants. Total phenolic and flavonoid contents correlated with antioxidant capacity, although structural factors also influenced activity. Importantly, all tested extracts and cold-pressed oil exhibited no mutagenic or genotoxic effects in the Ames/Salmonella assay. Overall, these findings provide a comprehensive characterization of S. altissimum and highlight its potential as a source of biologically active natural products.

PMID 42928286
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PubMedBioscience reports2026-10-25

Polyethylene glycol 35 preserves endothelial barrier integrity by stabilizing the glycocalyx and intercellular junctions.

Folch-Puy Emma E, Llaves-López Andrea A, Barnat-Cabrera Queralt Q, Manso-Álvarez Paula P et al.

Endothelial dysfunction is a hallmark of numerous inflammatory and ischemic conditions, characterized by increased permeability, disruption of intercellular junctions and endothelial glycocalyx (eGCX) degradation. In the present study, we investigated the ability of polyethylene glycol 35 (PEG35) to preserve endothelial barrier integrity in cultured human umbilical vein endothelial cells (HUVECs) exposed to inflammatory, thrombotic, hypoxia-mimetic and eGCX-disrupting stimuli. PEG35 mitigated the loss of cellular metabolic activity induced by apoptotic and hypoxia-mimetic stress. Functionally, PEG35 attenuated stimulus-induced increases in FITC-dextran permeability and helped maintain trans-endothelial electrical resistance (TEER) under pro-inflammatory and eGCX-disrupting agents. PEG35 also reduced LDH release and maintained higher TEER values in endothelial cells exposed to plasma collected from pancreas transplant recipients after reperfusion, which contained increased circulating levels of the endothelial glycocalyx component syndecan-1. Mechanistically, PEG35 reduced NFĸB p65 nuclear translocation under thrombin, TNFα, and hyaluronidase stimulation and attenuated inflammatory and endothelial activation-related transcriptional responses. PEG35 also modulated intercellular junction gene expression in a stimulus and target-dependent manner, helped maintain occludin and claudin-5 protein expression under selected injurious conditions, and limited the loss of eGCX-associated syndecan-1 and heparan sulfate staining after enzymatic degradation. Collectively, these findings support a multifactorial endothelial-protective effect of PEG35 involving preservation of endothelial surface layer, maintenance of junctional integrity and attenuation of inflammatory signalling. These results identify PEG35 as a potential vasoprotective candidate for conditions involving acute endothelial barrier injury.

PMID 42924999
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PubMedMinerva dental and oral science2026-10-25

Facial esthetic medicine in dentistry: botulinum toxin and hyaluronic acid fillers for smile-face harmonization.

Ballini Andrea A, Lo Muzio Lorenzo L, Giuliano Lucia L, Illuzzi Gaetano G et al.

Orofacial treatment planning is being redefined by the convergence of minimally invasive facial aesthetic medicine and aesthetic dentistry. Specifically, hyaluronic acid (HA) dermal fillers and botulinum toxin type A (BoNT-A) are being employed more frequently as adjuncts to maximize smile-lip-face harmony. The scope of non-invasive or minimally invasive facial aesthetic medicine for dentists has also been clarified by regulatory changes in Italy, underscoring the importance of competency-based training and organized risk management. The objective is to give a narrative summary of BoNT-A and HA fillers' indications, clinical procedures, integration into dental workflows, and safety concerns in dental practice, with a focus on perioral applications and complication management. In addition to focused searches in Google Scholar and important consensus texts (2000-2025; chosen updates through early 2026), a narrative search was carried out in PubMed/MEDLINE and Scopus. Systematic reviews, clinical trials, and expert consensus statements on face injectables and adverse event management were prioritized. There is evidence to support BoNT-A as a conservative adjunct for gummy smiles caused by hyperfunctional lip elevators, some lower-face dynamic rhytids, and masseter hypertrophy and bruxism-related myofascial pain, providing clinically meaningful reductions in pain, improvements in muscular and joint function, and favorable aesthetic outcomes. HA fillers may be used as a "finishing step" following orthodontic, periodontal, or restorative treatment to enhance lip contour and perioral soft-tissue support. Filler-induced vascular occlusion is the most important safety concern; early detection and prompt hyaluronidase treatment are essential, and ultrasound mapping is becoming more and more recommended for high-risk areas and tailored care. As an orofacial harmonization method, facial aesthetic medicine can be incorporated into modern dentistry as long as indications are conservative, patients are properly chosen and given consent, and clinics are prepared and trained to handle complications. Future studies should establish competency-based training pathways for dental professionals and standardize outcome measurements.

PMID 42922386
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PubMedDermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]2026-10-23

Hyaluronidase: A Call for High-Dosage Formulation in the United States.

Xia Joyce J, Cohen Joel L JL

PMID 42910821
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PubMedAnalytical chemistry2026-10-23

Catalytic Network states Govern Programmable Analytical Functions in a Multifunctional Nanozyme.

Liu Zhennian Z, Liu Zhixian Z, Yuan Jiali J, Yin Lingjun L et al.

Although multifunctional nanozymes enable diverse analytical applications, existing activity-based models cannot adequately explain how a single nanozyme is programmably reconfigured to perform distinct analytical functions under different reaction conditions. Here, we show that programmable analytical functions emerge from catalytic network states rather than isolated enzyme-like activities. Using hyaluronic acid-confined platinum nanozymes (HA-Pt) as a model system, we identify an autonomous chromogenic oxidation (ACO) process that proceeds without externally supplied H2O2. Mechanistic studies reveal that ACO emerges from localized coupling between oxygen activation and substrate oxidation within a confined polymeric microenvironment. Microenvironment disruption destabilizes the catalytic network state, whereas pH continuously redistributes catalytic pathway contributions to drive predictable state transitions. The resulting catalytic network states enable the same nanozyme platform to quantify total antioxidant capacity, uric acid, and hyaluronidase, thereby decoding complementary physiological dimensions of redox homeostasis, purine metabolism, and extracellular matrix remodeling. The strategy was validated using 22 clinical urine samples. This work establishes catalytic network state as a conceptual framework for programmable multifunctional analysis, shifting nanozyme design from activity engineering toward network-state engineering.

PMID 42916374
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PubMedProtein and peptide letters2026-10-22

Changes Associated with Hyaluronidase Enzyme in Skin Connective Tissue: An Experimental and Qualitative Study in Rats.

Tutak Fatma Nilay FN, Ozdemir Azimet A, Balik Ozan O, Bulbuloglu Semra S et al.

Hyaluronidase enzyme is frequently used by plastic surgeons in aesthetic procedures to break down hyaluronic acid. The potential benefits of hyaluronidase in the clinical management of conditions associated with diseases and aging in the skin connective tissue are a subject of ongoing research. In this study, we investigated the changes associated with the hyaluronidase enzyme injected subcutaneously into the dorsal region of rats in the skin connective tissue. This is an experimental and qualitative study. A total of 24 Wistar albino rats were divided into three groups of eight each: Control (Group 1), Sham (Group 2), and Experimental (Group 3). In the study, no procedure was performed on Group 1, normal saline was injected into Group 2, and hyaluronidase enzyme was injected subcutaneously into Group 3. At the end of the 14th day, sections were taken from the skin connective tissue of the injection site, and histochemical examination and biochemical analyses were performed on these sections. This research received no external funding. In Group 1, the collagen fibers, vessels, and layers of the epidermis and dermis appeared normal. In Group 2, the normal organization of collagen fibers was disrupted in some areas, and the connective tissue was edematous. In Group 3, a decrease in collagen fiber density in some areas, structural abnormalities in collagen and elastic fibers, and edema were detected. TGF-β1 and MMP-1 measurement results were compared between groups, and no statistically significant difference was found (p > 0.05). The results of this study indicate that the hyaluronidase enzyme is associated with a decrease in collagen fiber quantity, structural abnormalities in fibers, edema, and the development of impaired elastic fiber structures in skin connective tissue.

PMID 42906818
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