An Efficient, Lung-Targeted, Drug-Delivery System To Treat Asthma Via Microparticles

被引:12
|
作者
SreeHarsha, Nagaraja [1 ,2 ]
Venugopala, Katharigatta N. [1 ,3 ]
Nair, Anroop B. [1 ]
Roopashree, Teeka S. [4 ]
Attimarad, Mahesh [1 ]
Hiremath, Jagadeesh G. [2 ]
Al-Dhubiab, Bandar E. [1 ]
Ramnarayanan, Chandramouli [5 ]
Shinu, Pottathil [6 ]
Handral, Mukund [7 ]
Haroun, Micheline [1 ]
Tratrat, Christophe [1 ]
机构
[1] King Faisal Univ, Coll Clin Pharm, Dept Pharmaceut Sci, POB 400, Al Hasa, Saudi Arabia
[2] Vidya Siri Coll Pharm, Dept Pharmaceut, Bengaluru, India
[3] Durban Univ Technol, Dept Biotechnol & Food Technol, ZA-4001 Durban, South Africa
[4] Govt Coll Pharm, Dept Pharmacognosy, Bengaluru, India
[5] Krupanidhi Coll Pharm, Dept Qual Assurance, Bengaluru, India
[6] King Faisal Univ, Coll Clin Pharm, Dept Biomed Sci, Al Hasa, Saudi Arabia
[7] PES Univ, Fac Pharmaceut Sci, Dept Pharmacol, Bengaluru, India
来源
关键词
polylactic acid-co-glycolic acid; public health; spray dryer; microspheres; CHITOSAN MICROSPHERES; SPRAY DRYER; IN-VITRO; TISSUE DISTRIBUTION; RELEASE; NANOPARTICLES; NANO; PHARMACOKINETICS; NANOCAPSULE; METABOLISM;
D O I
10.2147/DDDT.S216660
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Chronic diseases such as diabetes, asthma, and heart disease are the leading causes of death in developing countries. Public health plays an important role in preventing such diseases to improve individuals' quality of life. Conventional dosage schemes used in public health to cure various diseases generally lead to undesirable side effects and renders the overall treatment ineffective. For example, a required concentration of drug cannot reach the lungs using conventional methods to cure asthma. Microspheres have emerged as a confirmed drug-delivery system to cure asthma. Method: In this paper, a salbutamol-loaded poly lactic acid-co-glycolic acid-polyethylene glycol (PLGA-PEG) microsphere (SPP)-based formulation was prepared using a Buchi B-90 nanospray drier. Face-centered central composite design (CCD) was applied to optimize the spray-drying process. Results: The drug content and product yield were found to be 72%+/- 0.8% and 86%+/- 0.4%, respectively; drug release (91.1%) peaked for up to 12 hrs in vitro. Microspheres obtained from the spray dryer were found to be shriveled. The experiments were carried out and verified using various groups of rabbits. In our study, the particle size (8.24 mu m) was observed to be an essential parameter for drug delivery. The in vivo results indicated that the targeting efficacy and drug concentration in the lung was higher with the salbutamolloaded PLGA-PEG SPP formulation (1,410.1 +/- 10.11 mu g/g, 15 mins), as compared to the conventional formulation (92 +/- 0.56 mu g/g, 10 min). The final product was stable under 5 degrees C +/- 2 degrees C, 25 degrees C +/- 2 degrees C, and 40 degrees C +/- 2 degrees C/75%+/- 5% relative humidity. In addition, these co-polymers have a good safety profile, as determined by testing on human alveolar basal epithelium A549 cell lines. Conclusion: Our results prove that microspheres are an alternative drug-delivery system for lung-targeted asthma treatments used in public health.
引用
收藏
页码:4389 / 4403
页数:15
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