Partial tablet coating by 3D printing

被引:16
作者
Tsintavi, Eleni [1 ]
Rekkas, Dimitrios M. [1 ]
Bettini, Ruggero [2 ]
机构
[1] Natl & Kapodistrian Univ Athens, Dept Pharm, Athens 15784, Greece
[2] Univ Parma, Food & Drug Dept, Parco Area Sci 27-A, I-43124 Parma, Italy
关键词
3D printing; Tablet coating; Design of experiments; DRUG-RELEASE; FORMULATIONS; FABRICATION; MECHANISMS; INDUSTRY;
D O I
10.1016/j.ijpharm.2020.119298
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the last decade 3D printing (3DP) technology has gained increasing interest in the pharmaceutical field addressing several novel challenges such as on-demand manufacturing at the point of need, customization of drug release profiles and patient-specific solutions as well as combinations of several APIs in one dosage form. Therefore, 3DP can become a new and promising path to drug product development and manufacturing, able to support specific therapies and improve compliance, safety and effectiveness. The aim of this work was to partially coat tablets with a glyceride, namely Precirol ATO 5 using a semi-solids 3D printer as an approach for tuning the release of two Active Pharmaceutical Ingredients (APIs), the hydrophilic methyl-levodopa hydrochloride (Melevodopa) and the lipophilic Acyclovir. Various parameters of the 3DP coating process were purposefully modified using experimental design techniques in order to customize the selected APIs release profile, without affecting the core composition of the formulation. The percentage of the tablet surface coated, the number of coating layers as well as the coated sides of the tablet where the parameters which controlled the release profile for both APIs. Different dissolution profiles have been achieved by tuning these simple parameters, which revealed a non-Fickian release mechanism regardless of the API.
引用
收藏
页数:15
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[1]   Emergence of 3D Printed Dosage Forms: Opportunities and Challenges [J].
Alhnan, Mohamed A. ;
Okwuosa, Tochukwu C. ;
Sadia, Muzna ;
Wan, Ka-Wai ;
Ahmed, Waqar ;
Arafat, Basel .
PHARMACEUTICAL RESEARCH, 2016, 33 (08) :1817-1832
[2]  
Alice Konta Andrea, 2017, Bioengineering-Basel, V4, P79, DOI 10.3390/bioengineering4040079
[3]  
[Anonymous], [No title captured]
[4]  
[Anonymous], [No title captured]
[5]  
[Anonymous], [No title captured]
[6]  
APRECIA, 2015, FDA APPR 1 3D PRINT
[7]   Tablet fragmentation without a disintegrant: A novel design approach for accelerating disintegration and drug release from 3D printed cellulosic tablets [J].
Arafat, Basel ;
Wojsz, Magdalena ;
Isreb, Abdullah ;
Forbes, Robert T. ;
Isreb, Mohammad ;
Ahmed, Waqar ;
Arafat, Tawfiq ;
Alhnan, Mohamed A. .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2018, 118 :191-199
[8]   The Digital Pharmacies Era: How 3D Printing Technology Using Fused Deposition Modeling Can Become a Reality [J].
Araujo, Maisa R. P. ;
Sa-Barreto, Livia L. ;
Gratieri, Tais ;
Gelfuso, Guilherme M. ;
Cunha-Filho, Marcilio .
PHARMACEUTICS, 2019, 11 (03)
[9]   The rise of 3-D printing: The advantages of additive manufacturing over traditional manufacturing [J].
Attaran, Mohsen .
BUSINESS HORIZONS, 2017, 60 (05) :677-688
[10]   Rapid prototyping or rapid production? 3D printing processes move industry towards the latter [J].
Bak, D .
ASSEMBLY AUTOMATION, 2003, 23 (04) :340-345