3D printed dispersible efavirenz tablets: A strategy for nasogastric administration in children

被引:3
|
作者
Funk, Nadine Lysyk [1 ,2 ,3 ]
Januskaite, Patricija [3 ]
Beck, Ruy Carlos Ruver [1 ,2 ]
Basit, Abdul W. [3 ,4 ,5 ]
Goyanes, Alvaro [3 ,4 ,5 ,6 ,7 ]
机构
[1] Univ Fed Rio Grande do Sul, Fac Farm, Programa Posgrad Ciencias Farmaceut, Porto Alegre, Brazil
[2] Univ Fed Rio Grande do Sul UFRGS, Fac Farm, Lab Nanocarreadores & Impressao 3D Tecnol Farmaceu, Porto Alegre, Brazil
[3] UCL, UCL Sch Pharm, Dept Pharmaceut, 29-39 Brunswick Sq, London WC1N 1AX, England
[4] FABRX Ltd, Henwood House, Ashford TN24 8DH, Kent, England
[5] FABRX Artificial Intelligence, Carretera Escairon 14, Currelos 27543, O Savinao, Spain
[6] Univ Santiago de Compostela, Fac Farm, Dept Farmacol Farm & Tecnol Farmaceut, Inst Mat iMATUS,ID Farma GI 1645, Santiago De Compostela 15782, Spain
[7] Univ Santiago de Compostela, Hlth Res Inst Santiago de Compostela IDIS, Santiago De Compostela 15782, Spain
基金
英国工程与自然科学研究理事会;
关键词
Additive manufacturing of oral drug products; Enteral route administration of medicines; Nasogastric tubes and ostomies; Printed formulations and drug delivery systems; Powder bed fusion 3D printing pharmaceuticals; Pediatrics and acceptability;
D O I
10.1016/j.ijpharm.2024.124299
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Enteral feeding tubes (EFTs) can be placed in children diagnosed with HIV which need nutritional support due to malnutrition. EFTs are the main route for medication administration in these patients, bringing up concerns about off label use of medicines, dose inaccuracy and tube clogging. Here we report for the first time the use of selective laser sintering (SLS) 3D printing to develop efavirenz (EFZ) dispersible printlets for patients with HIV that require EFT administration. Water soluble polymers Parteck (R) MXP and Kollidon (R) VA64 were used to obtain both 500 mg (P500 and K500) and 1000 mg printlets (P1000 and K1000) containing 200 mg of EFZ each. The use of SLS 3D printing obtained porous dosage forms with high drug content (20 % and 40 % w/w) and drug amorphization using both polymers. P500, K500 and K1000 printlets reached disintegration in under 230 s in 20 mL of water (25 +/- 1 degrees C), whilst P1000 only partially disintegrated, possibly due to saturation of the polymer in the medium. As a result, the development of dispersible EFZ printlets using hydrophilic polymers can be explored as a potential strategy for drug delivery through EFTs in paediatrics with HIV, paving the way towards the exploration of more rapidly disintegrating polymers and excipients for SLS 3D printing.
引用
收藏
页数:8
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