Discharge Mode Enhances the Energy Efficiency of Radiofrequency Microneedle: An In Vivo Porcine Study of Optimized Histological Responses Under Constant Total Energy

IF 3.5 4区 医学 Q2 DERMATOLOGY
Jiayi Feng, Xuelai Wang, Ling Zhang, Shize Ma, Lvping Huang
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Abstract

Objective

To explore the immediate histological effects of insulated (IMRF) and non-insulated (NMRF) radiofrequency microneedles across different discharge modes under a constant total energy, and to evaluate long-term collagen remodeling specifically in the classical discharge mode.

Methods

The backs of Bama pigs (n = 3) were assigned to the classical and sequential discharge modes under IMRF and NMRF treatments at a fixed total energy (1000 mJ). The classical discharge mode group was set as follows: high power and short pulse width (Group A), medium power and medium pulse width (Group B), low power and long pulse width (Group C), and the sequential discharge mode group (ultra-high power and ultra-short pulse width). IMRF and NMRF were used for treatment. The microthermal zone (MTZ) was evaluated and quantified by hematoxylin and eosin (HE) staining immediately after the treatment. Three months after the procedure, the skin lesions were extracted, and the mRNA expression of collagen type I and III was quantitatively evaluated by real-time PCR.

Results

Under the classical discharge mode with constant total energy delivery, a higher power level in IMRF resulted in greater MTZ density (p = 0.014), whereas no significant differences were observed in the depth and width of sub-damage lesions and coagulation zones. In contrast, NMRF failed to produce typical MTZs under any of the three parameter settings. At the 3-month follow-up, type I collagen expression was significantly upregulated in both A and B groups of IMRF (I-A p = 0.002, I-B p = 0.001), while type III collagen expression showed no notable change among all groups (p = 0.671). Under the sequential discharge mode, a sharp increase in single-needle peak power led to the formation of dense MTZs in both IMRF and NMRF. Compared with the medium-power classic mode in the classical discharge mode, the sequential discharge mode resulted in significantly higher MTZ density (IMRF p = 0.002; NMRF p = 0.011). Furthermore, the sub-damage lesion depth was significantly greater with IMRF than with NMRF (NMRF vs. I-B p = 0.017; NMRF vs. IMRF p = 0.01).

Conclusion

MTZ formation is highly dependent on the per-needle power threshold rather than the total energy applied, and is closely associated with the upregulation of type I collagen. The sequential discharge mode, via a “high-power ultrashort pulse width” mechanism, effectively overcomes the activation thresholds of both IMRF and NMRF without increasing the overall thermal load. By generating denser and more stable MTZs, it exhibits promising clinical potential, representing a pivotal direction for future MRF optimization.

放电方式提高射频微针的能量效率:恒定总能量下优化组织反应的猪体内研究
目的探讨恒定总能量下不同放电模式下绝缘(IMRF)和非绝缘(NMRF)射频微针的即时组织学效应,并评价经典放电模式下胶原蛋白的长期重塑。方法选取巴马猪(n = 3)的背部,分别在固定总能量(1000 mJ)的IMRF和NMRF处理下进行经典和顺序放电。经典放电模式组设置为:高功率短脉宽组(A组)、中功率中脉宽组(B组)、低功率长脉宽组(C组)和顺序放电模式组(超高功率超短脉宽)。采用IMRF和NMRF治疗。处理后立即用苏木精和伊红(HE)染色评价和定量微热区(MTZ)。术后3个月提取皮损,实时荧光定量PCR检测ⅰ型和ⅲ型胶原mRNA表达。结果在总能量恒定的经典放电模式下,高功率的IMRF导致MTZ密度增大(p = 0.014),而亚损伤区和凝血区深度和宽度无显著差异。相比之下,NMRF在三种参数设置下都不能产生典型的MTZs。随访3个月,IMRF A组和B组I型胶原表达均显著上调(I-A p = 0.002, I-B p = 0.001),而各组间III型胶原表达无显著变化(p = 0.671)。在顺序放电模式下,单针峰值功率的急剧增加导致IMRF和NMRF中形成密集的MTZs。与经典放电模式下的中功率经典模式相比,顺序放电模式导致MTZ密度显著提高(IMRF p = 0.002; NMRF p = 0.011)。此外,IMRF组亚损伤深度明显大于NMRF组(NMRF vs I-B p = 0.017; NMRF vs IMRF p = 0.01)。结论MTZ的形成高度依赖于每针功率阈值而非总能量,与I型胶原蛋白的上调密切相关。顺序放电模式通过“高功率超短脉冲宽度”机制,有效地克服了IMRF和NMRF的激活阈值,而不会增加总热负荷。通过生成更密集、更稳定的MTZs,显示出良好的临床潜力,代表了未来MRF优化的关键方向。
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来源期刊
CiteScore
4.30
自引率
13.00%
发文量
818
审稿时长
>12 weeks
期刊介绍: The Journal of Cosmetic Dermatology publishes high quality, peer-reviewed articles on all aspects of cosmetic dermatology with the aim to foster the highest standards of patient care in cosmetic dermatology. Published quarterly, the Journal of Cosmetic Dermatology facilitates continuing professional development and provides a forum for the exchange of scientific research and innovative techniques. The scope of coverage includes, but will not be limited to: healthy skin; skin maintenance; ageing skin; photodamage and photoprotection; rejuvenation; biochemistry, endocrinology and neuroimmunology of healthy skin; imaging; skin measurement; quality of life; skin types; sensitive skin; rosacea and acne; sebum; sweat; fat; phlebology; hair conservation, restoration and removal; nails and nail surgery; pigment; psychological and medicolegal issues; retinoids; cosmetic chemistry; dermopharmacy; cosmeceuticals; toiletries; striae; cellulite; cosmetic dermatological surgery; blepharoplasty; liposuction; surgical complications; botulinum; fillers, peels and dermabrasion; local and tumescent anaesthesia; electrosurgery; lasers, including laser physics, laser research and safety, vascular lasers, pigment lasers, hair removal lasers, tattoo removal lasers, resurfacing lasers, dermal remodelling lasers and laser complications.
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