Formulation, Optimization, and Evaluation of Non-Propellent Foam-Based Formulation for Burn Wounds Treatment

被引:0
|
作者
Kumar, Mohit [1 ]
Chopra, Shruti [1 ]
Mahmood, Syed [2 ]
Mirza, Mohd Aamir [3 ]
Bhatia, Amit [1 ]
机构
[1] Maharaja Ranjit Singh Punjab Tech Univ MRSPTU, Dept Pharmaceut Sci & Technol, Bathinda 151001, Punjab, India
[2] Univ Malaya, Fac Pharm, Dept Pharmaceut Technol, Kuala Lumpur 50603, Malaysia
[3] Sch Pharmaceut Educ & Res, Dept Pharmaceut, New Delhi, India
关键词
Non-propellent foam; Foam collapse time; Foam density; Topical drug delivery; Antibacterial activity; BUBBLE-SIZE; DESIGN; COMPOSITE; PSORIASIS; RELEASE;
D O I
10.1016/j.xphs.2024.07.004
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Burn injuries worldwide pose significant health risks due to frequent microbial infections, which worsen complications and increase mortality rates. The conventional antimicrobial formulations are available in the form of ointments and creams. These formulations are very greasy and stick to the clothes. The applications of these formulations by finger or applicator produce pain in the affected area and incur the possibility of microbial infection. To overcome these hurdles, authors developed a novel non-propellent foam (NPF) based formulation containing chlorhexidine for effective topical delivery. Initially, NPF containing Labrasol (R) (26.7%), sodium lauryl sulfate (1.2%), hydroxy propyl methyl cellulose (0.56%), butylated hydroxytoluene (0.1%), ethanol (1%), and distilled water was prepared and assessed for its consistency, and ability to form foam. The NPF was statistically optimized using the Box-Behnken design to determine the effect of polymer and surfactants on the critical foam properties. The optimized formulation showed a collapse time of 45 s with a unique nature of collapsing upon slight touch which is highly beneficial for burn patients with microbial infection. The diffusion study showed that more than 90% of the drug was released within 6 h. The skin permeation study showed that 23% of the total drug permeated through the skin after 6 h with 7.64 mu g/cm(2)/h permeation flux. The developed formulation showed good antibacterial activity. The minimum inhibitory concentration of prepared NPF was found to be 2.5 mu g/mL, 2.5 mu g/mL, and 5.0 mu g/mL against E. coli (MTCC-1687), P. aeruginosa (MTCC-1688), and S aureus (MTCC-737) respectively. The developed NPF formulation showed quick collapse time, excellent spreadability, good anti-bacterial activity, and a non-sticky nature representing a promising avenue for burn wound treatment without using any applicator.
引用
收藏
页码:2795 / 2807
页数:13
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