Flynn Timothy Corcoran
Department of Dermatology, University of North Carolina, Chapel Hill, NC 27514, USA.
Dermatol Clin. 2004 Apr;22(2):207-11, vii. doi: 10.1016/s0733-8635(03)00070-6.
Myobloc is the currently available commercial formulation of type B botulinum toxin. Released in the United States in 2000, it is approved by the Food and Drug Administration for the treatment of cervical dystonia. The most commonly used botulinum toxins, the type A toxins (Botox and Dysport), affect the SNAP-25 protein, whereas the type B toxin (Myobloc) affects vesicle-associated membrane protein, also known as synaptobrevin. Both type B and type A are antigenically distinct. This article explains the difference between Myobloc and type A toxins, reviews equivalency and other published studies, and describes practical uses for this product in facial aesthetics.
Myobloc是目前可用的B型肉毒杆菌毒素商业制剂。2000年在美国上市,它被美国食品药品监督管理局批准用于治疗颈部肌张力障碍。最常用的肉毒杆菌毒素,即A型毒素(保妥适和Dysport),作用于SNAP - 25蛋白,而B型毒素(Myobloc)作用于囊泡相关膜蛋白,也称为突触结合蛋白。B型和A型在抗原性上均不同。本文解释了Myobloc与A型毒素之间的差异,回顾了等效性及其他已发表的研究,并描述了该产品在面部美学中的实际应用。