Lipid Engineered Nanoparticle Therapy for Burn Wound Treatment

被引:2
作者
Qadir, Abdul [1 ]
Ahmad, Usama [2 ]
Ali, Asad [2 ]
Shahid, Aisha [2 ]
Aqil, Mohd [1 ]
Khan, Nausheen [1 ]
Ali, Athar [3 ]
Almalki, Waleed H. [4 ]
Alghamdi, Saad [5 ]
Abul Barkat, Md [6 ]
Beg, Sarwar [1 ,7 ,8 ]
机构
[1] Jamia Hamdard New Delhi, Dept Pharmaceut, Sch Pharmaceut Educ & Res, New Delhi, India
[2] Integral Univ, Fac Pharm, Lucknow, Uttar Pradesh, India
[3] Jamia Hamdard, Dept Biotechnol, Ctr Transgen Plant Dev, New Delhi, India
[4] Umm Al Qura Univ, Coll Pharm, Dept Pharmacol & Toxicol, Mecca, Saudi Arabia
[5] Umm Al Qura Univ, Fac Appl MedicalSci, Lab Med Dept, Mecca, Saudi Arabia
[6] Univ Hafr Al Batin, Coll Pharm, Dept Pharmaceut, Hafar al Batin 39524, Saudi Arabia
[7] Univ Cent Lancashire, Fac Clin & Biomed Sci, Sch Pharm & Biomed Sci, Al Jamiah 39524, Hafr Al Batin, Saudi Arabia
[8] Univ Cent Lancashire, Fac Clin & Biomed Sci, Sch Pharm & Biomed Sci, Preston PR1 2HE, Lancs, England
关键词
Burn; injury; nanoparticles; lipids; wound healing; liposomes; niosomes; ethosomes; TOPICAL ANTIMICROBIAL AGENTS; CONTROLLED DRUG-DELIVERY; FIBROBLAST-GROWTH-FACTOR; SILVER SULFADIAZINE; CUBIC PHASE; SURFACTANT NANOEMULSION; HEALTH OUTCOMES; INFECTION; CARE; MANAGEMENT;
D O I
10.2174/1389201022666210823110532
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Skin is the largest organ of the human body protecting the underlying organs and tissues from any foreign attack. Any damage caused in the skin may sometimes result in serious consequences within the internal body tissues. Burn is one such issue that damages the layers of the skin and thereby making the skin vulnerable and prone to any foreign matter entering and causing serious diseases. Methods: An online literature assessment was steered for the lipid nanoparticles, burn wound treatments, and different types of nanoformulation. Appropriate information was taken from different electronic scientific databases such as Web of Science, Elsevier, Science Direct, Springer, PubMed, Google Scholar etc. Additional data was summarized from textbooks, local prints and scripts. Results: Recent innovations and developments in nanotechnology-based drug delivery systems have shown promising results in minimizing the drawbacks associated with conventional therapies. Lipid based nanoparticles possess capabilities to deliver active agents to their target site without the possibility of degradation. Conventional therapy of burn wound is costly and the treatment is long lasting, making the patient uncomfortable. Moreover, it also doesn't yield satisfactory results or narrow effects. Encapsulation of bioactives inside the lipid core protects the active entity from pH and enzymatic degradations. Conclusion: This review highlights the drawbacks associated with conventional dosage forms. A lot of consideration is focused on the advancement of nanomaterials using innovative methods in wound care for treating burn wounds with a faster healing effect. This review article highlights recent developments in lipid based nanoformulations for the treatment of burn wound injury.
引用
收藏
页码:1449 / 1459
页数:11
相关论文
共 92 条
[41]   Opioid-Induced Hyperalgesia and Burn Pain [J].
Holtman, Joseph R., Jr. ;
Jellish, W. Scott .
JOURNAL OF BURN CARE & RESEARCH, 2012, 33 (06) :692-701
[42]   Fungal wound infection (not colonization) is independently associated with mortality in burn patients [J].
Horvath, Edward E. ;
Murray, Clinton K. ;
Vaughan, George M. ;
Chung, Kevin K. ;
Hospenthal, Duane R. ;
Wade, Charles E. ;
Holcomb, John B. ;
Wolf, Steven E. ;
Mason, Arthur D., Jr. ;
Cancio, Leopoldo C. .
ANNALS OF SURGERY, 2007, 245 (06) :978-985
[43]  
Hussain Z, 2020, MICRO NANO TECHNOL, P141, DOI 10.1016/B978-0-12-816960-5.00009-4
[44]   Fibroblast growth factor 2 facilitates the differentiation of transplanted bone marrow cells into hepatocytes [J].
Ishikawa, T ;
Terai, S ;
Urata, Y ;
Marumoto, Y ;
Aoyama, K ;
Sakaida, I ;
Murata, T ;
Nishina, H ;
Shinoda, K ;
Uchimura, S ;
Hamamoto, Y ;
Okita, K .
CELL AND TISSUE RESEARCH, 2006, 323 (02) :221-231
[45]   Microbiological findings in burn patients treated in a general versus a designated intensive care unit: Effect on length of stay [J].
Issler-Fisher, Andrea C. ;
Fakin, Richard M. ;
Fisher, Oliver M. ;
McKew, Genevieve ;
Gazzola, Riccardo ;
Rauch, Ann-Kathrin ;
Gottlieb, Thomas ;
Haertsch, Peter ;
Guggenheim, Merlin ;
Giovanoli, Pietro ;
Maitz, Peter K. M. .
BURNS, 2016, 42 (08) :1805-1818
[46]   Adapalene loaded solid lipid nanoparticles gel: An effective approach for acne treatment [J].
Jain, Amit K. ;
Jain, Ashay ;
Garg, Neeraj K. ;
Agarwal, Abhinav ;
Jain, Atul ;
Jain, Som Akshay ;
Tyagi, Rajeev K. ;
Jain, Rakesh K. ;
Agrawal, Himanshu ;
Agrawal, Govind P. .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2014, 121 :222-229
[47]   Pathophysiologic response to severe burn injury [J].
Jeschke, Marc G. ;
Chinkes, David L. ;
Finnerty, Celeste C. ;
Kulp, Gabriela ;
Suman, Oscar E. ;
Norbury, William B. ;
Branski, Ludwik K. ;
Gauglitz, Gerd G. ;
Mlcak, Ronald P. ;
Herndon, David N. .
ANNALS OF SURGERY, 2008, 248 (03) :387-400
[48]   Burn injury [J].
Jeschke, Marc G. ;
van Baar, Margriet E. ;
Choudhry, Mashkoor A. ;
Chung, Kevin K. ;
Gibran, Nicole S. ;
Logsetty, Sarvesh .
NATURE REVIEWS DISEASE PRIMERS, 2020, 6 (01)
[49]   Long-Term Persistance of the Pathophysiologic Response to Severe Burn Injury [J].
Jeschke, Marc G. ;
Gauglitz, Gerd G. ;
Kulp, Gabriela A. ;
Finnerty, Celeste C. ;
Williams, Felicia N. ;
Kraft, Robert ;
Suman, Oscar E. ;
Mlcak, Ronald P. ;
Herndon, David N. .
PLOS ONE, 2011, 6 (07)
[50]  
Jeschke MG, 2012, HDB BURNS ACUTE BURN, P1, DOI [10.1007/978-3-7091-0348-7, DOI 10.1007/978-3-7091-0348-7]