Repeat application of microneedles does not alter skin appearance or barrier function and causes no measurable disturbance of serum biomarkers of infection, inflammation or immunity in mice in vivo

被引:82
作者
Vicente-Perez, Eva M. [1 ]
Larraneta, Eneko [1 ]
McCrudden, Maeliosa T. C. [1 ]
Kissenpfennig, Adrien [2 ]
Hegarty, Shauna [3 ]
McCarthy, Helen O. [1 ]
Donnelly, Ryan F. [1 ]
机构
[1] Queens Univ Belfast, Sch Pharm, 97 Lisburn Rd, Belfast BT9 7BL, Antrim, North Ireland
[2] Queens Univ Belfast, Sch Med Dent & Biomed Sci, Ctr Expt Med, Wellcome Wolfson Bldg,97 Lisburn Rd, Belfast BT9 7BL, Antrim, North Ireland
[3] Royal Victoria Hosp, 274 Grosvenor Rd, Belfast BT12 6BA, Antrim, North Ireland
关键词
Microneedles; Repeat application; Skin barrier function; Biomarkers; Regulatory; C-REACTIVE PROTEIN; TRANSDERMAL DRUG-DELIVERY; NECROSIS-FACTOR-ALPHA; HAIRLESS MOUSE; SAFETY; ARRAYS; INTERLEUKIN-1; LIFETIME; DISEASE;
D O I
10.1016/j.ejpb.2017.04.029
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We address, for the first time, the impact of skin insertion on multiple occasions of polymeric microneedle arrays in an animal model in vivo. Dissolving microneedle arrays prepared from aqueous blends of 20% w/w Gantrez (R) S-97 BF and 40% w/w poly(vinyl pyrrolidone) 58 kDa and hydrogel-forming microneedle arrays prepared from aqueous blends of and poly(ethyleneglycol) 10 kDa were repeatedly applied to the skin of hairless mice in vivo. Skin appearance and skin barrier function, as illustrated by measurement of transepidermal water loss, were not measurably altered during the entire study period. Biomarkers of infection, immunity and inflammation/irritation were also statistically unchanged, regardless of the microneedle formulation, needle density or number of applications. Mice remained healthy throughout and continued to gain weight during the study. For example, transepidermal water loss values were typically in the range 10-15 g m(-2) h(-1) immediately prior to microneedle insertion and 15-25 g m(-2) h(-1) immediately following microneedle removal, regardless of when they were measured during the study periods. Serum biomarker levels, measured immediately post-mortem were always in the range 10-20 mu g ml(-1) for C-reactive protein, 0.5-1.5 mg ml(-1) for Immunoglobulin G and 1000-2500 pg ml(-1) for interleukin 1-beta and were never statistically different from untreated controls. No measurable levels of tumour necrosis factor-alpha were found in any animals. These findings are encouraging for the formulations investigated, suggesting that their repeated use by patients will not cause undesirable side-effects. By beginning to address potential regulatory questions at an early stage, the microneedles field will be ideally-placed to take advantage of the potential market. This work illustrates a potential pre-clinical strategy for development of regulatory dossiers on microneedle technologies. (C) 2017 The Author. Published by Elsevier B.V.
引用
收藏
页码:400 / 407
页数:8
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