Institute of Pharmaceutical Science, King's College London, London SE1 9NH, United Kingdom; Department of Forensic Evidence and Criminology, U.A.E., Dubai, Dubai Police HQ, Al Tawar 1, United Arab Emirates.
Applied DNA Sciences, Stony Brook, NY 11790, USA.
Int J Pharm. 2019 Nov 25;571:118656. doi: 10.1016/j.ijpharm.2019.118656. Epub 2019 Sep 6.
The licensed pharmaceutical industry and regulators use many approaches to control counterfeiting, but it remains a very difficult task to differentiate between counterfeit and real products. Moreover, there is a lack of techniques available for providing a batch specific molecular bar code for tablets that has the required traceability, specificity and sensitivity to be fit for purpose. The aim of this study was to evaluate DNA molecular tags as a potential anti-counterfeiting technology in tablets. Lactose tablets (400 mg) were used as a model to investigate incorporation DNA molecular tag into a solid dosage form: DNA authentication was carried out on an Applied DNA SigNify® qPCR instrument. Tablet batches were subjected to accelerated stability conditions (40 °C and 75% RH) for up to 6 months. All batches passed the monograph specifications of the British Pharmacopoeia (hardness, friability and mass uniformity) throughout the storage period. In all of recovery plots, the number of cycles required for DNA detection (Cq values) increased as a function of storage time, which indicated a reduction in tag levels, but it should be noted for all storage experiments the tag was clearly detected. It would appear that DNA molecular tags could feasibly be applied within the pharmaceutical development cycle when a new solid dosage form is brought to the market so as to mitigate the risk and dangers of counterfeiting.
许可制药行业和监管机构采用了许多方法来控制假药,但要区分假药和真药仍然是一项非常困难的任务。此外,缺乏可用于为片剂提供具有所需可追溯性、特异性和灵敏度的批次特定分子条码的技术,以达到预期目的。本研究旨在评估 DNA 分子标签作为片剂防伪技术的潜力。乳糖片(400mg)被用作模型来研究将 DNA 分子标签掺入固体制剂中:在 Applied DNA SigNify® qPCR 仪器上进行 DNA 验证。将片剂批次置于加速稳定性条件(40°C 和 75% RH)下长达 6 个月。在整个储存期内,所有批次均通过英国药典(硬度、脆性和质量均匀性)专论规格。在所有回收图中,DNA 检测所需的循环数(Cq 值)随储存时间的增加而增加,这表明标签水平降低,但应注意,在所有储存实验中,均清晰检测到标签。似乎当新的固体制剂投放市场时,可以在制药开发周期中实际应用 DNA 分子标签,以减轻假药的风险和危害。