|Source:||The roots of Radix ophiopogonis.|
|Biological Activity or Inhibitors:|
|Solvent:||DMSO, Pyridine, Methanol, Ethanol, etc.|
|Storage:||Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: firstname.lastname@example.org
|After receiving:||The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.|
|1 mg||5 mg||10 mg||20 mg||25 mg|
|1 mM||2.2297 mL||11.1483 mL||22.2965 mL||44.5931 mL||55.7414 mL|
|5 mM||0.4459 mL||2.2297 mL||4.4593 mL||8.9186 mL||11.1483 mL|
|10 mM||0.223 mL||1.1148 mL||2.2297 mL||4.4593 mL||5.5741 mL|
|50 mM||0.0446 mL||0.223 mL||0.4459 mL||0.8919 mL||1.1148 mL|
|100 mM||0.0223 mL||0.1115 mL||0.223 mL||0.4459 mL||0.5574 mL|
J Pharm Biomed Anal. 2016 Jan 5;117:61-72.
|Global analysis of chemical constituents in Shengmai injection using high performance liquid chromatography coupled with tandem mass spectrometry.[Pubmed: 26342447]|
|This study aimed to develop a specific and reliable method to comprehensively analyze the chemical constituents in Shengmai injection (SMI) using high performance liquid chromatography coupled with tandem mass spectrometry. The qualitative analysis of SMI was achieved on a Kromasil 100-5C18 column, and the results demonstrated that a total of sixty-two compounds in SMI were unambiguously assigned or tentatively identified, and further, twenty-one compounds including fourteen saponins, six lignans and one L-Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside were quantified by HPLC-MS. Furthermore, L-Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside, originated from Radix ophiopogonis, was identified and quantified in SMI for the first time. The method validation results indicated that the methods were simple, specific and reliable. All the investigated compounds showed good linearity (r(2)≥0.9992) with a relatively wide concentration range and acceptable recovery at 90.13-109.09%. Consequently, the developed methods were successfully applied to ten batches of SMI samples analysis. The proposed methods may provide a useful and comprehensive reference for the quality control of SMI, and thus to provide supporting data for the quality control and application of SMI clinically.|