Pulmonary drug delivery devices and nanosystems as potential treatment strategies for acute respiratory distress syndrome (ARDS)

被引:10
作者
Dhege, Clarence T. [1 ]
Kumar, Pradeep [1 ]
Choonara, Yahya E. [1 ]
机构
[1] Univ Witwatersrand, Fac Hlth Sci, Wits Adv Drug Delivery Platform Res Unit, Dept Pharm & Pharmacol,Sch Therapeut Sci, 7 York Rd, ZA-2193 Parktown, South Africa
基金
新加坡国家研究基金会; 英国医学研究理事会;
关键词
Acute respiratory distress syndrome (ARDS); Drug delivery systems; Pulmonary delivery; Aerosol; Nanoparticles; ACUTE LUNG INJURY; METABOLIZING-ENZYMES; N-ACETYLCYSTEINE; INHALER; SYSTEMS; NANOPARTICLES; NANOCARRIERS; TRANSPORTERS; MACROPHAGES; FORMULATION;
D O I
10.1016/j.ijpharm.2024.124182
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite advances in drug delivery technologies, treating acute respiratory distress syndrome (ARDS) is challenging due to pathophysiological barriers such as lung injury, oedema fluid build-up, and lung inflammation. Active pharmaceutical ingredients (API) can be delivered directly to the lung site of action with the use of aerosol -based drug delivery devices, and this circumvents the hepatic first -pass effect and improves the bioavailability of drugs. This review discusses the various challenges and barriers for pulmonary drug delivery, current interventions for delivery, considerations for effective drug delivery, and the use of nanoparticle drug delivery carriers as potential strategies for delivering therapeutics in ARDS. Nanosystems have the added benefit of entrapping drugs, increase pulmonary drug bioavailability, and using biocompatible and biodegradable excipients that can facilitate targeted and/or controlled delivery. These systems provide an alternative to existing conventional systems. An effective way to deliver drugs for the treatment of ARDS can be by using colloidal systems that are aerosolized or inhaled. Drug distribution to the deeper pulmonary tissues is necessary due to the significant endothelial cell destruction that is prevalent in ARDS. The particle size of nanoparticles (<0.5 mu m) makes them ideal candidates for treating ARDS as they can reach the alveoli. A look into the various potential benefits and limitations of nanosystems used for other lung disorders is also considered to indicate how they may be useful for the potential treatment of ARDS.
引用
收藏
页数:22
相关论文
共 170 条
[1]  
Agu RU, 2001, RESP RES, V2, P198
[2]   Liposomes or Extracellular Vesicles: A Comprehensive Comparison of Both Lipid Bilayer Vesicles for Pulmonary Drug Delivery [J].
Al-Jipouri, Ali ;
Almurisi, Samah Hamed ;
Al-Japairai, Khater ;
Bakar, Latifah Munirah ;
Doolaanea, Abd Almonem .
POLYMERS, 2023, 15 (02)
[3]   Experimental Study of Spiriva Respimat Soft Mist Inhaler Spray Characterization: Size Distributions and Velocity [J].
Alatrash, Abubaker ;
Mehri, Rym ;
Ogrodnik, Nicholas ;
Matida, Edgar ;
Fiorenza, Frank .
JOURNAL OF AEROSOL MEDICINE AND PULMONARY DRUG DELIVERY, 2019, 32 (05) :293-302
[4]  
Almalki W. H., 2022, Microbiome in Inflammatory Lung Diseases, P1, DOI [10.1007/978-981-16-8957-41, DOI 10.1007/978-981-16-8957-41]
[5]  
Anderson Paula, 2006, Int J Chron Obstruct Pulmon Dis, V1, P251
[6]   Current Pharmacological Approach to ARDS: The Place of Bosentan [J].
Araz, Omer .
EURASIAN JOURNAL OF MEDICINE, 2020, 52 (01) :81-85
[7]   Investigational pharmacological agents for the treatment of ARDS [J].
Aribindi, Katyayini ;
Lim, Michelle ;
Lakshminrusimha, Satyan ;
Albertson, Timothy .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2024, 33 (03) :243-277
[8]   Dendrimers as a carrier for pulmonary delivery of enoxaparin, a low-molecular weight heparin [J].
Bai, Shuhua ;
Thomas, Chandan ;
Ahsan, Fakhrul .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 96 (08) :2090-2106
[9]   Surfactant-mediated dissolution: Contributions of solubility enhancement and relatively low micelle diffusivity [J].
Balakrishnan, A ;
Rege, BD ;
Amidon, GL ;
Polli, JE .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 93 (08) :2064-2075
[10]   Pulmonary pathology of ARDS in COVID-19: A pathological review for clinicians [J].
Batah, Sabrina Setembre ;
Fabro, Alexandre Todorovic .
RESPIRATORY MEDICINE, 2021, 176