Method for preparing octreotide and octreotide acetate
An octreotide and desalting technology, applied in the field of biopharmaceuticals, can solve the problems of complex preparation process and low yield, and achieve the effect of optimizing the production process
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Embodiment 1
[0035] Embodiment 1 (HPLC method detects angiotensin crude product raw material and purification intermediate solution purity and quantification)
[0036] Instrument: Waters2695 / 2489 high performance liquid chromatography
[0037] Separation column: Waters XBridge-C18, 4.6×150mm, 5μm
[0038] Mobile phase: A is 20mM NaH 2 PO 4 -H 3 PO 4(pH3.0), B is 50% aqueous acetonitrile solution by volume percentage
[0039] Flow rate is 1.0mL / min, detection wavelength is 220nm, room temperature detection,
[0040] The elution gradient is shown in Table 1 below, and the percentages are volume percentages.
[0041] Table 1 Mobile phase elution gradient
[0042] Elution step
Embodiment 2
[0043] Embodiment 2 (75mm inner diameter L&L4003 preparative column packing)
[0044] Using Load&Lock dynamic axial compression and static locking technology, the filler is styrene-divinylbenzene copolymer (reversed phase packing Agilent PLRP-S), the pore size is 10nm, the particle size is 10μm, and the column packing density is 0.33g / mL. Bed pressure 650psi, using Varian chromatographic packing system, 370g dry powder filler, 2L methanol after stirring and homogenizing, poured into 75mm inner diameter L&L4003 preparative column, compression ratio is 3:1, carrier gas is N 2 , adjust the carrier gas pressure so that the oil pressure gauge pressure is 2000psi, and the dynamic axial compression to the height of the column bed is 26cm, which is used as the preparative column for the reverse-phase purification and reverse-phase desalination scheme.
Embodiment 3
[0046] (1) Reversed-phase purification of crude angiotensin raw materials
[0047] Instrument: Varian SD-1 high pressure liquid phase preparation system
[0048] Chromatographic column: self-packed preparative column Load&Lock400375×260mm in Example 2, PLRP-S10μm10nm
[0049] Mobile phase: A is a 0.1% trifluoroacetic acid aqueous solution by volume, B is a 0.1% trifluoroacetic acetonitrile solution by volume, angiotensin crude product (angiotensin synthesized by solid-phase method disclosed in patent application CN201210131066.5) Crude product) through the acetonitrile aqueous solution of volume percent 5% is that solvent is dissolved and is mixed with 10g / L solution, sample liquid is mobile phase C after filtration clarification, measures its HPLC purity by the method for Example 1 and is 84.98%, and retention time is 10.34min , the HPLC data are shown in Table 2.
[0050] Table 2 The peak results of angiotensin crude product HPLC detection
[0051] Peak ID
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