METHOD FOR RAPID ON-SITE DETECTION OF FENTANYL ANALOGS USING A MINIATURE MASS SPECTROMETER

Abstract

The present invention discloses a method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer, comprising the following steps: (1) selecting a spotting plate; (2) loading a sample: depositing the sample and 3-nitrobenzonitrile solution in acetonitrile on the spotting plate to form a crystalline mixture; (3) carrying out analysis and detection: setting the parameters of the miniature mass spectrometer, placing the crystalline mixture on the spotting plate in close proximity to the inlet of the miniature mass spectrometer, and facilitating the ionization of the crystalline mixture for the analysis and detection of fentanyl analogs. The method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer provided by the present invention requires no extraction solvent, no voltage, no laser, no gas, and the method is simple, rapid, and suitable for rapid on-site detection of fentanyl analogs.

Description

FIELD OF THE INVENTION

The present invention relates to a method for detection of chemical substances, especially a method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer.

BACKGROUND OF THE INVENTION

Fentanyl is an opioid receptor agonist synthesized by a Belgian scientist named Paul Janssen in 1960, having a chemical name of N[1-(2-phenethyl)-4-piperidiny]-N-phenylpropionamide. With the analgesic effect 80 times than that of morphine, fentanyl is commonly used for anesthesia during and after surgery. Fentanyl analogs are formed by modification of the parent substance (fentanyl) and are composed of three parts: phenylalkyl, piperidinyl ring, and propylalkylamide. Fentanyl analogs include remifentanil, carfentanil, sufentanil, etc., the analgesic effect of which is normally higher than that of fentanyl. For example, the analgesic effect of carfentanil is 100 times than that of fentanyl and 10,000 times than that of morphine.

Fentanyl analogs have powerful analgesic effect, short onset time, and are easily accessible. However, their excessive use may lead to physical and mental dependence, respiratory depression, and even death. In recent years, the abuse of fentanyl and fentanyl analogs has continued worldwide, causing a large number of casualties and seriously impairing social stability. Within just four months from the end of 2015 to the beginning of 2016, Sweden reported seven deaths due to the overdose of fentanyl analogs; in the same year, five deaths were caused by overdose of fentanyl analogs in Ohio of USA. With the increasing number of deaths, the prevention and control of fentanyl analogs are urgent. On May 1, 2019, the Ministry of Public Security, National Health Commission, and State Food and Drug Administration of China listed fentanyl analogs in the Supplementary Catalogue of Controlled Varieties of Non-Medicinal Narcotic Drugs and Psychotropic Substances, implementing whole-class control for fentanyl analogs.

SUMMARY OF THE INVENTION

The technical problem to be solved by the present invention is to provide a simple, fast, and sustainable method that is suitable for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer. The studies of the present invention include the investigations of the types of fentanyl analogs, ionization modes of chemical analytes, and detection conditions of ambient ionization and miniature mass spectrometer.

A method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer, comprising the following steps:

(1) selecting a spotting plate;

(2) loading a sample: depositing the sample and 3-nitrobenzonitrile solution in acetonitrile on the spotting plate to form a crystalline mixture;

(3) carrying out analysis and detection: setting the parameters of the miniature mass spectrometer, placing the crystalline mixture on the spotting plate in close proximity to the inlet of the miniature mass spectrometer, and facilitating the ionization of the crystalline mixture for the analysis and detection of fentanyl analogs;

wherein the sample includes powder, blood, and sweat; there are 49 kinds of fentanyl analogs, and the analysis parameters of the miniature mass spectrometer and limits of detection (LODs) in step (3) are shown in Table 1;

TABLE 1
The analysis parameters of the miniature mass spectrometer and limits of detection (LODs) for the 49 fentanyl analogs
	Ionization
Fentanyl analogs	mode	m/z	RF/kHz	AC/kHz	CID-AC/kHz	CID-AC/Vpp	LOD/(μg/kg)
fentanyl	positive	337	150-800	5-46	47	220	20
para-flufentanyl	positive	355	150-880	5-42	43	220	20
meta-flufentanyl	positive	355	150-860	5-43	44	220	20
ortho-flufentanyl	positive	355	150-860	5-42	43	210	20
N-phenyl-N-[1-[2-(2-thienyl)ethyl]-	positive	343	150-840	5-44	45	220	50
4-piperidyl]propanamide
acetylfentanyl	positive	323	150-780	5-45	46	210	50
N-(2-fluorophenyl)-N-(1-	positive	341	150-820	5-44	45	215	20
phenethylpiperidin-4-yl)acetamide
N-(3-fluorophenyl)-N-(1-	positive	341	150-820	5-44	45	220	20
phenethylpiperidin-4-yl)acetamide
N-(4-fluorophenyl)-N-[1-(2-	positive	341	150-820	5-44	45	220	20
phenylethyl)-4-piperidinyl]-
acetamide
butyrfentanyl	positive	351	150-830	5-43	44	235	50
isobutyryl fentanyl	positive	351	150-840	5-42	43	222	50
4-fluorobutyrfentanyl	positive	369	150-900	5-40	41	225	50
meta-fluorobutyryl fentanyl	positive	369	150-880	5-40	41	220	50
N-(2-fluorophenyl)-N-(1-	positive	369	150-880	5-40	41	220	50
phenethylpiperidin-4-yl)butyramide
para-fluoroisobutyrfentanyl	positive	369	150-880	5-40	41	220	50
cis-3-methylfentanyl	positive	351	150-850	5-43	44	223	50
trans-3-methylfentanyl	positive	351	150-850	5-43	44	221	50
alpha-methylfentanyl	positive	351	150-850	5-43	44	220	50
N-[1-[1-methyl-2-(2-thienyl)ethyl]-4-	positive	357	150-870	5-42	43	217	100
piperidyl]-N-phenylpropanamide
cis-3-methylthiofentanyl	positive	357	150-880	5-42	43	215	100
2-methoxy-N-phenyl-N-[1-(2-	positive	353	150-840	5-43	44	210	20
phenylethyl)-4-piperidinyl]-
acetamide
para-methoxy acetyl fentanyl	positive	353	150-840	5-42	43	220	20
N-(2-fluorophenyl)-N-(1-	positive	353	150-820	5-43	44	215	20
phenethylpiperidin-4-yl)acrylamide
N-[1-(2-hydroxy-2-phenylethyl)-4-	positive	353	150-840	5-42	43	220	200
piperidyl]-N-phenylpropanamide
norfentanyl	positive	232	150-600	5-67	68	180	50
acrylfentanyl	positive	335	150-820	5-44	45	220	50
methyl-4-(N-phenylpropionamido)-	positive	395	150-930	5-36	37	200	100
1-phenethylpiperidine-4-carboxylate
furanylfentanyl	positive	375	150-920	5-40	41	205	50
valerylfentanyl	positive	365	150-900	5-40	41	225	50
ocfentanil	positive	371	150-880	5-40	41	215	50
remifentanil	positive	377	150-940	5-39	40	180	200
sufentanyl	positive	387	150-950	5-37	38	190	100
alfentanil	positive	417	150-1000	5-34	35	200	200
N-phenyl-N-(1-phenethylpiperidin-4-	positive	379	150-940	5-38	39	205	50
yl)tetrahydrofuran-2-carboxamide
heptanoyl fentanyl	positive	394	150-920	5-36	37	225	50
phenyl fentanyl	positive	385	150-950	5-38	39	210	20
hexanoyl fentanyl	positive	380	150-940	5-38	39	230	50
N-phenyl-N-(1-(2-(thiophen-2-	positive	329	150-800	5-45	46	215	100
yl)ethyl)piperidin-4-yl)acetamide
N-(1-(2-hydroxy-2-(thiophen-2-	positive	359	150-890	5-41	42	213	200
yl)ethyl)piperidin-4-yl)-N-
phenylpropanamide
meta-fluoro methoxyacetyl fentanyl	positive	371	150-890	5-40	41	200	50
acetyl-alpha-methylfentanyl	positive	337	150-800	5-44	45	226	20
para-methoxy methoxyacetyl	positive	383	150-910	5-38	39	210	50
fentanyl
beta-hydroxy-3-methylfentanyl	positive	367	150-900	5-40	41	225	50
para-methoxy acryl fentanyl	positive	365	150-900	5-40	41	220	50
para-methoxy tetrahydrofuran	positive	409	150-920	5-35	36	210	20
cyclopentyl fentanyl	positive	378	150-890	5-39	40	210	50
thiophene fentanyl	positive	392	150-920	5-37	38	210	50
1-phenethyl-4-piperidone	positive	204	150-500	5-76	77	220	20
1-phenethyl-N-phenylpiperidin-4-	positive	281	150-670	5-55	56	230	20
amine

wherein the spotting plate is a triangular paper substrate.

According to the method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer, wherein: step (2) specifically comprises the following steps: transferring 1-3 μL of liquid sample or 1-3 μg of powder sample to the spotting plate, depositing 5-10 μL of the 3-nitrobenzonitrile solution in acetonitrile at a concentration of 100 μg/μL on the sample, and exposing to air for 10-30 seconds to form a crystalline mixture.

According to the method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer, wherein: in step (3), the crystalline mixture on the spotting plate was placed in close proximity to the inlet of the miniature mass spectrometer for 1-5 seconds, and the crystalline mixture was expected to produce charged particles upon sublimation due to the intrinsic vacuum at the inlet aperture of the miniature mass spectrometer.

According to the method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer, wherein: the base and height of the triangular paper substrate are 1 cm and 1.5 cm, respectively.

The difference between the method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer of the present invention and the prior art lies in that: the method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer provided by the present invention requires no extraction solvent, no voltage, no laser, no gas, and the method is simple, rapid, and suitable for rapid on-site detection of fentanyl analogs.

The inventiveness and advantages of the present invention are as follows:

1. For the first time, the present invention proposes a method combining matrix-assisted ionization and miniature mass spectrometry for rapid on-site detection of fentanyl analogs in suspicious powders or unknown liquids and the detection time is short;

2. The present invention does not need the uses of extraction solvent, voltage, laser or gas;

3. The types of samples involved in the present invention include: powder, blood, urine, sweat, etc.

4. The substances involved in the present invention include: 49 kinds of fentanyl analogs.

The method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer according to the present invention will be further described below with reference to the accompanying drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

Additional objectives, functions, and advantages of the present invention will be set forth in the description of embodiments which follow, with reference to the accompanying drawings in which:

FIG. 1 is the schematic diagram of the selection of an optimal spotting plate according to the present invention;

FIG. 2 is the MS/MS spectrum of fentanyl;

FIG. 3 is the MS/MS spectrum of para-flufentanyl;

FIG. 4 is the MS/MS spectrum of meta-flufentanyl;

FIG. 5 is the MS/MS spectrum of ortho-flufentanyl;

FIG. 6 is the MS/MS spectrum of N-phenyl-N-[1-[2-(2-thienyl)ethyl]-4-piperidyl]propanamide;

FIG. 7 is the MS/MS spectrum of acetylfentanyl;

FIG. 8 is the MS/MS spectrum of N-(2-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)acetamide;

FIG. 9 is the MS/MS spectrum of N-(3-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)acetamide;

FIG. 10 is the MS/MS spectrum of N-(4-fluorophenyl)-N-[1-(2-phenylethyl)-4-piperidinyl]-acetamide;

FIG. 11 is the MS/MS spectrum of butyrfentanyl;

FIG. 12 is the MS/MS spectrum of isobutyryl fentanyl;

FIG. 13 is the MS/MS spectrum of 4-fluorobutyrfentanyl;

FIG. 14 is the MS/MS spectrum of meta-Fluorobutyryl fentanyl;

FIG. 15 is the MS/MS spectrum of N-(2-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)butyramide;

FIG. 16 is the MS/MS spectrum of para-fluoroisobutyrfentanyl;

FIG. 17 is the MS/MS spectrum of cis-3-Methylfentanyl;

FIG. 18 is the MS/MS spectrum of trans-3-methylfentanyl;

FIG. 19 is the MS/MS spectrum of alpha-methylfentanyl;

FIG. 20 is the MS/MS spectrum of N[1-[1-Methyl-2-(2-thienyl)ethyl]-4-piperidyl]-N-phenylpropanamide;

FIG. 21 is the MS/MS spectrum of cis-3-methylthiofentanyl;

FIG. 22 is the MS/MS spectrum of 2-methoxy-N-phenyl-N[1-(2-phenylethyl)-4-piperidinyl]-acetamide;

FIG. 23 is the MS/MS spectrum ofpara-methoxy acetyl fentanyl;

FIG. 24 is the MS/MS spectrum of N-(2-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)acrylamide;

FIG. 25 is the MS/MS spectrum of N[1-(2-hydroxy-2-phenylethyl)-4-piperidyl]-N-phenylpropanamide;

FIG. 26 is the MS/MS spectrum of norfentanyl;

FIG. 27 is the MS/MS spectrum of acrylfentanyl;

FIG. 28 is the MS/MS spectrum of methyl-4-(N-phenylpropionamido)-1-phenethylpiperidine-4-carboxylate;

FIG. 29 is the MS/MS spectrum of furanylfentanyl;

FIG. 30 is the MS/MS spectrum of valerylfentanyl;

FIG. 31 is the MS/MS spectrum of ocfentanil;

FIG. 32 is the MS/MS spectrum of remifentanil;

FIG. 33 is the MS/MS spectrum of sufentanyl;

FIG. 34 is the MS/MS spectrum of alfentanil;

FIG. 35 is the MS/MS spectrum of N-phenyl-N-(1-phenethylpiperidin-4-yl)tetrahydrofuran-2-carboxamide;

FIG. 36 is the MS/MS spectrum of heptanoyl fentanyl;

FIG. 37 is the MS/MS spectrum of phenyl fentanyl;

FIG. 38 is the MS/MS spectrum of hexanoyl fentanyl;

FIG. 39 is the MS/MS spectrum of N-phenyl-N-(1-(2-(thiophen-2-yl)ethyl)piperidin-4-yl)acetamide;

FIG. 40 is the MS/MS spectrum of N-(1-(2-hydroxy-2-(thiophen-2-ypethyl)piperidin-4-yl)-N-phenylpropanamide;

FIG. 41 is the MS/MS spectrum of meta-fluoro methoxyacetyl fentanyl;

FIG. 42 is the MS/MS spectrum of acetyl-alpha-methylfentanyl;

FIG. 43 is the MS/MS spectrum ofpara-methoxy methoxyacetyl fentanyl;

FIG. 44 is the MS/MS spectrum of beta-hydroxy-3-methylfentanyl;

FIG. 45 is the MS/MS spectrum ofpara-methoxy acryl fentanyl;

FIG. 46 is the MS/MS spectrum ofpara-methoxy tetrahydrofuran fentanyl;

FIG. 47 is the MS/MS spectrum of cyclopentyl fentanyl;

FIG. 48 is the MS/MS spectrum of thiophene fentanyl;

FIG. 49 is the MS/MS spectrum of 1-phenethyl-4-piperidone;

FIG. 50 is the MS/MS spectrum of 1-phenethyl-N-phenylpiperidin-4-amine.

DETAILED DESCRIPTION OF THE INVENTION

1. Apparatus and Materials

Mini β miniature mass spectrometer: PURSPEC Technologies (Beijing, China). 3-nitrobenzonitrile, CAS number 619-24-9, molecular formula C₇H₄N₂O₂, and average molecular weight 148.12 g/mol.

2. Analysis and Detection Method

A method for rapid on-site detection of fentanyl analogs in suspicious powder or liquid samples using a miniature mass spectrometer includes the following steps:

(1) selecting a spotting plate: choosing a triangular paper substrate as the spotting plate, with a base of 1 cm and a height of 1.5 cm;

(2) loading a sample: loading 1-3 μL of liquid sample (or 1-3 μg of powder sample) to a tip of the triangular paper substrate, adding 5-10 μL of the 3-nitrobenzonitrile solution in acetonitrile on the spotting plate, and exposing to air for 10-30 seconds to form a crystalline mixture of the sample and 3-nitrobenzonitrile;

(3) carrying out analysis and detection: setting the parameters of the miniature mass spectrometer, placing the crystalline mixture on the spotting plate in close proximity to the inlet of the miniature mass spectrometer for 1-5 seconds, and facilitating the ionization of the crystalline mixture for the analysis and detection of fentanyl analogs.

There are 49 kinds of fentanyl analogs, and analysis parameters of the miniature mass spectrometer and LODs are as shown in Table 1;

TABLE 1
The analysis parameters of the miniature mass spectrometer and limits of detection (LODs) for the 49 fentanyl analogs
	Ionization
Fentanyl analogs	mode	m/z	RF/kHz	AC/kHz	CID-AC/kHz	CID-AC/Vpp	LOD/(μg/kg)
fentanyl	positive	337	150-800	5-46	47	220	20
para-flufentanyl	positive	355	150-880	5-42	43	220	20
meta-flufentanyl	positive	355	150-860	5-43	44	220	20
ortho-flufentanyl	positive	355	150-860	5-42	43	210	20
N-phenyl-N-[1-[2-(2-thienyl)ethyl]-	positive	343	150-840	5-44	45	220	50
4-piperidyl]propanamide
acetylfentanyl	positive	323	150-780	5-45	46	210	50
N-(2-fluorophenyl)-N-(1-	positive	341	150-820	5-44	45	215	20
phenethylpiperidin-4-yl)acetamide
N-(3-fluorophenyl)-N-(1-	positive	341	150-820	5-44	45	220	20
phenethylpiperidin-4-yl)acetamide
N-(4-fluorophenyl)-N-[1-(2-	positive	341	150-820	5-44	45	220	20
phenylethyl)-4-piperidinyl]-
acetamide
butyrfentanyl	positive	351	150-830	5-43	44	235	50
isobutyryl fentanyl	positive	351	150-840	5-42	43	222	50
4-fluorobutyrfentanyl	positive	369	150-900	5-40	41	225	50
meta-fluorobutyryl fentanyl	positive	369	150-880	5-40	41	220	50
N-(2-fluorophenyl)-N-(1-	positive	369	150-880	5-40	41	220	50
phenethylpiperidin-4-yl)butyramide
para-fluoroisobutyrfentanyl	positive	369	150-880	5-40	41	220	50
cis-3-methylfentanyl	positive	351	150-850	5-43	44	223	50
trans-3-methylfentanyl	positive	351	150-850	5-43	44	221	50
alpha-methylfentanyl	positive	351	150-850	5-43	44	220	50
N-[1-[1-methyl-2-(2-thienyl)ethyl]-4-	positive	357	150-870	5-42	43	217	100
piperidyl]-N-phenylpropanamide
cis-3-methylthiofentanyl	positive	357	150-880	5-42	43	215	100
2-methoxy-N-phenyl-N-[1-(2-	positive	353	150-840	5-43	44	210	20
phenylethyl)-4-piperidinyl]-
acetamide
para-methoxy acetyl fentanyl	positive	353	150-840	5-42	43	220	20
N-(2-fluorophenyl)-N-(1-	positive	353	150-820	5-43	44	215	20
phenethylpiperidin-4-yl)acrylamide
N-[1-(2-hydroxy-2-phenylethyl)-4-	positive	353	150-840	5-42	43	220	200
piperidyl]-N-phenylpropanamide
norfentanyl	positive	232	150-600	5-67	68	180	50
acrylfentanyl	positive	335	150-820	5-44	45	220	50
methyl-4-(N-phenylpropionamido)-	positive	395	150-930	5-36	37	200	100
1-phenethylpiperidine-4-carboxylate
furanylfentanyl	positive	375	150-920	5-40	41	205	50
valerylfentanyl	positive	365	150-900	5-40	41	225	50
ocfentanil	positive	371	150-880	5-40	41	215	50
remifentanil	positive	377	150-940	5-39	40	180	200
sufentanyl	positive	387	150-950	5-37	38	190	100
alfentanil	positive	417	150-1000	5-34	35	200	200
N-phenyl-N-(1-phenethylpiperidin-4-	positive	379	150-940	5-38	39	205	50
yl)tetrahydrofuran-2-carboxamide
heptanoyl fentanyl	positive	394	150-920	5-36	37	225	50
phenyl fentanyl	positive	385	150-950	5-38	39	210	20
hexanoyl fentanyl	positive	380	150-940	5-38	39	230	50
N-phenyl-N-(1-(2-(thiophen-2-	positive	329	150-800	5-45	46	215	100
yl)ethyl)piperidin-4-yl)acetamide
N-(1-(2-hydroxy-2-(thiophen-2-	positive	359	150-890	5-41	42	213	200
yl)ethyl)piperidin-4-yl)-N-
phenylpropanamide
meta-fluoro methoxyacetyl fentanyl	positive	371	150-890	5-40	41	200	50
acetyl-alpha-methylfentanyl	positive	337	150-800	5-44	45	226	20
para-methoxy methoxyacetyl	positive	383	150-910	5-38	39	210	50
fentanyl
beta-hydroxy-3-methylfentanyl	positive	367	150-900	5-40	41	225	50
para-methoxy acryl fentanyl	positive	365	150-900	5-40	41	220	50
para-methoxy tetrahydrofuran	positive	409	150-920	5-35	36	210	20
cyclopentyl fentanyl	positive	378	150-890	5-39	40	210	50
thiophene fentanyl	positive	392	150-920	5-37	38	210	50
1-phenethyl-4-piperidone	positive	204	150-500	5-76	77	220	20
1-phenethyl-N-phenylpiperidin-4-	positive	281	150-670	5-55	56	230	20
amine

TABLE 2
The information on the 49 fentanyl analogs
Name	molecular formula	molecular weight
fentanyl hydrochloride	C22H28N2O•HCl	372.94
para-fluorofentanyl hydrochloride	C22H27FN2O•HCl	390.93
meta-fluorofentanyl hydrochloride	C22H27FN2O•HCl	390.93
ortho-fluorofentanyl hydrochloride	C22H27FN2O•HCl	390.93
N-phenyl-N-[1-[2-(2-thienyl)ethyl]-4-piperidyl]propanamide	C20H26N2OS•HCl	378.96
hydrochloride
acetyl fentanyl	C21H26N2O	322.44
N-(2-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)acetamide	C21H25FN2O•HCl	376.90
hydrochloride
N-(3-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)acetamide	C21H25FN2O•HCl	376.90
hydrochloride
N-(4-fluorophenyl)-N-[1-(2-phenylethyl)-4-piperidinyl]-	C21H25FN2O•HCl	376.90
acetamide, hydrochloride
butyrfentanyl hydrochloride	C23H30N2O•HCl	386.96
isobutyryl fentanyl	C23H30N2O	350.50
4-fluorobutyrfentanyl	C23H29FN2O	368.49
meta-fluorobutyryl fentanyl hydrochloride	C23H29FN2O•HCl	404.95
N-(2-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)butyramide	C23H29FN2O•HCl•H2O	422.97
hydrochloride hydrate
p-fluoroisobutyrfentanyl	C23H29FN2O•HCl	404.95
cis-3-methylfentanyl hydrochloride	C23H30N2O•HCl	386.96
trans-3-methylfentanyl hydrochloride	C23H30N2O•HCl	386.96
alpha-methylfentanyl hydrochloride	C23H30N2O•HCl	386.96
N-[1-[1-methyl-2-(2-thienyl)ethyl]-4-piperidyl]-N-phenylpropanamide	C21H28N2OS•HCl	392.99
hydrochloride
cis-3-methylthiofentanyl hydrochloride	C21H28N2OS•HCl	392.99
2-methoxy-N-phenyl-N-[1-(2-phenylethyl)-4-piperidinyl]-acetamide	C22H28N2O2•HCl	388.94
hydrochloride
para-methoxy Acetyl fentanyl hydrochloride hemihydrate	C22H28N2O2•HCl•0.5H2O	397.94
N-(2-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)acrylamide	C22H25FN2O•HCl	388.91
hydrochloride
N-[1-(2-hydroxy-2-phenylethyl)-4-piperidyl]-N-phenylpropanamide	C22H28N2O2•HCl	388.94
hydrochloride
norfentanyl hydrochloride hydrate	C14H20N2O•HCl•H2O	286.80
acrylfentanyl	C22H26N2O	334.46
methyl-4-(N-phenylpropionamido)-1-phenethylpiperidine-4-	C24H30N2O3•HCl	430.97
carboxylate hydrochloride
furanylfentanyl	C24H26N2O2	374.48
valerylfentanyl	C24H32N2O	364.53
ocfentanil	C22H27FN2O2	370.46
remifentanil hydrochloride	C20H28N2O5•HCl	412.91
sufentanyl	C22H30N2O2S	386.55
alfentanil hydrochloride	C21H32N6O3•HCl	452.98
N-phenyl-N-(1-phenethylpiperidin-4-yl)tetrahydrofuran-2-carboxamide	C24H30N2O2•HCl•0.5H2O	423.98
hydrochloride hemihydrate
heptanoyl fentanyl hydrochloride	C26H36N2O•HCl	429.05
phenyl fentanyl hydrochloride	C26H28N2O•HCl	420.98
hexanoyl fentanyl hydrochloride	C25H34N2O•HCl	415.02
N-phenyl-N-(1-(2-(thiophen-2-yl)ethyl)piperidin-4-yl)acetamide	C19H24N2OS•HCl	364.93
hydrochloride
N-(1-(2-hydroxy-2-(thiophen-2-yl)ethyl)piperidin-4-yl)-N-	C20H26N2O2S•HCl	394.96
phenylpropanamide hydrochloride
meta-fluoro Methoxyacetyl fentanyl hydrochloride	C22H27FN2O2•HCl	406.93
acetyl-alpha-methylfentanyl hydrochloride	C22H28N2O•HCl	372.94
para-methoxy methoxyacetyl fentanyl hydrochloride	C23H30N2O3•HCl	418.96
beta-hydroxy-3-methylfentanyl hydrochloride	C23H30N2O2•HCl	402.96
para-methoxy acryl fentanyl hydrochloride	C23H28N2O2•HCl	400.95
para-methoxy tetrahydrofuran fentanyl	C25H32N2O3	408.54
cyclopentyl fentanyl hydrochloride	C25H32N2O•HCl	412.99
thiophene fentanyl hydrochloride	C24H26N2OS•HCl	427.00
1-phenethyl-4-piperidone	C13H17NO	203.28
1-phenethyl-N-phenylpiperidin-4-amine dihydrochloride hydrate	C19H24N2•2HCl•H2O	371.35
Note:
Part of the 49 fentanyl analogs exist in the form of hydrochloride or hydrated hydrochloride.

FIG. 2 is the MS/MS spectrum of fentanyl;

FIG. 3 is the MS/MS spectrum of para-flufentanyl;

FIG. 4 is the MS/MS spectrum of meta-flufentanyl;

FIG. 5 is the MS/MS spectrum of ortho-flufentanyl;

FIG. 6 is the MS/MS spectrum of N-phenyl-N-[1-[2-(2-thienyl)ethyl]-4-piperidyl]propanamide;

FIG. 7 is the MS/MS spectrum of acetylfentanyl;

FIG. 8 is the MS/MS spectrum of N-(2-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)acetamide;

FIG. 9 is the MS/MS spectrum of N-(3-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)acetamide;

FIG. 10 is the MS/MS spectrum of N-(4-fluorophenyl)-N-[1-(2-phenylethyl)-4-piperidinyl]-acetamide;

FIG. 11 is the MS/MS spectrum of butyrfentanyl;

FIG. 12 is the MS/MS spectrum of isobutyryl fentanyl;

FIG. 13 is the MS/MS spectrum of 4-fluorobutyrfentanyl;

FIG. 14 is the MS/MS spectrum of meta-Fluorobutyryl fentanyl;

FIG. 15 is the MS/MS spectrum of N-(2-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)butyramide;

FIG. 16 is the MS/MS spectrum ofpara-fluoroisobutyrfentanyl;

FIG. 17 is the MS/MS spectrum of cis-3-Methylfentanyl;

FIG. 18 is the MS/MS spectrum of trans-3-methylfentanyl;

FIG. 19 is the MS/MS spectrum of a/pha-methylfentanyl;

FIG. 20 is the MS/MS spectrum of N[1-[1-Methyl-2-(2-thienyl)ethyl]-4-piperidyl]-N-phenylpropanamide;

FIG. 21 is the MS/MS spectrum of cis-3-methylthiofentanyl;

FIG. 22 is the MS/MS spectrum of 2-methoxy-N-phenyl-N[1-(2-phenylethyl)-4-piperidinyl]-acetamide;

FIG. 23 is the MS/MS spectrum ofpara-methoxy acetyl fentanyl;

FIG. 24 is the MS/MS spectrum of N-(2-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)acrylamide;

FIG. 25 is the MS/MS spectrum of N[1-(2-hydroxy-2-phenylethyl)-4-piperidyl]-N-phenylpropanamide;

FIG. 26 is the MS/MS spectrum of norfentanyl;

FIG. 27 is the MS/MS spectrum of acrylfentanyl;

FIG. 28 is the MS/MS spectrum of methyl-4-(N-phenylpropionamido)-1-phenethylpiperidine-4-carboxylate;

FIG. 29 is the MS/MS spectrum of furanylfentanyl;

FIG. 30 is the MS/MS spectrum of valerylfentanyl;

FIG. 31 is the MS/MS spectrum of ocfentanil;

FIG. 32 is the MS/MS spectrum of remifentanil;

FIG. 33 is the MS/MS spectrum of sufentanyl;

FIG. 34 is the MS/MS spectrum of alfentanil;

FIG. 35 is the MS/MS spectrum of N-phenyl-N-(1-phenethylpiperidin-4-yl)tetrahydrofuran-2-carboxamide;

FIG. 36 is the MS/MS spectrum of heptanoyl fentanyl;

FIG. 37 is the MS/MS spectrum of phenyl fentanyl;

FIG. 38 is the MS/MS spectrum of hexanoyl fentanyl;

FIG. 39 is the MS/MS spectrum of N-phenyl-N-(1-(2-(thiophen-2-yl)ethyl)piperidin-4-yl)acetamide;

FIG. 40 is the MS/MS spectrum of N-(1-(2-hydroxy-2-(thiophen-2-yl)ethyl)piperidin-4-yl)-N-phenylpropanamide;

FIG. 41 is the MS/MS spectrum of meta-fluoro methoxyacetyl fentanyl;

FIG. 42 is the MS/MS spectrum of acetyl-alpha-methylfentanyl;

FIG. 43 is the MS/MS spectrum ofpara-methoxy methoxyacetyl fentanyl;

FIG. 44 is the MS/MS spectrum of beta-hydroxy-3-methylfentanyl;

FIG. 45 is the MS/MS spectrum ofpara-methoxy acryl fentanyl;

FIG. 46 is the MS/MS spectrum ofpara-methoxy tetrahydrofuran fentanyl;

FIG. 47 is the MS/MS spectrum of cyclopentyl fentanyl;

FIG. 48 is the MS/MS spectrum of thiophene fentanyl;

FIG. 49 is the MS/MS spectrum of 1-phenethyl-4-piperidone;

FIG. 50 is the MS/MS spectrum of 1-phenethyl-N-phenylpiperidin-4-amine.

A method for the detection of fentanyl in blood:

The experimental protocols described in the following embodiments are conventional methods unless otherwise specified. The reagents and materials can be obtained from commercial sources unless otherwise specified. The reference standards of fentanyl analogs were purchased from Shanghai Yuansi Biaowu Technology Co., Ltd.

Step 1: Preparation of Positive Sample

A standard solution of the fentanyl was added to the artificial blood. Positive artificial blood sample was prepared by adding 10 μL of the standard solution of fentanyl at a concentration of 100 μg/μL to 1 mL of artificial blood.

Step 2: Sample Deposition

Aliquots of 2 μL of positive sample were deposited onto the tip of the triangular paper substrate, 6 μL of the 3-nitrobenzonitrile solution in acetonitrile at a concentration of 100 μg/μLt (5 mg of 3-nitrobenzonitrile solid dissolved in 50 μL acetonitrile) was deposited, and the mixture was allowed to expose to air for 30 seconds.

Step 3: Ambient Ionization

The parameters of the miniature mass spectrometer were set according to the data in Table 1, and the crystalline mixture on the tip of the triangular paper substrate was placed in close proximity to the inlet of the miniature mass spectrometer for 3 seconds for analysis and detection. The mass spectrum is shown in FIG. 2.

The invention optimizes the selection of the spotting plates. Under the same experimental conditions, a filter paper, a triangular paper substrate, a glass slide, an aluminum foil, a centrifuge tube cap or a cotton swab were investigated as different spotting plates. The signal intensities of the miniature mass spectrometer were compared. The experiments were conducted in 6 replicates for each kind of spotting plates, and the average results were compared. The data were normalized and compared, and the results were shown in FIG. 1. It can be seen from FIG. 1 that when the triangular paper substrate was selected as the spotting plate, the mass spectrometric signal was the most intensive, so the triangular paper substrate was selected as the optimal spotting plate.

The foregoing embodiments are merely illustrative of preferred embodiments of the present invention and are not intended to limit the scope of the present invention. Various variations and modifications made to the technical solutions of the present invention by those skilled in the art without departing from the spirit of the present invention are embraced in the protection scope of the present invention as defined by the appended claims.

Claims

1. A method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer, comprising the following steps: (1) selecting a spotting plate;(2) loading a sample: depositing the sample and 3-nitrobenzonitrile solution in acetonitrile on the spotting plate to form a crystalline mixture;(3) carrying out analysis and detection: setting the parameters of the miniature mass spectrometer, placing the crystalline mixture on the spotting plate in close proximity to the inlet of the miniature mass spectrometer, and facilitating the ionization of the crystalline mixture for the analysis and detection of fentanyl analogs;wherein the sample comprises powder, blood, and sweat; there are 49 kinds of fentanyl analogs, and the analysis parameters of the miniature mass spectrometer and LODs in step (3) are as shown in Table 1;

2. The method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer according to claim 1, wherein: step (2) specifically comprises the following steps: transferring 1-3 μL of liquid sample or 1-3 μg of powder sample to the spotting plate, depositing 5-10 μL of the 3-nitrobenzonitrile solution in acetonitrile at a concentration of 100 μg/μL on the sample, and exposing to air for 10-30 seconds to form a crystalline mixture.

3. The method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer according to claim 2, wherein: in step (3), the crystalline mixture on the spotting plate was placed in close proximity to the inlet of the miniature mass spectrometer for 1-5 seconds, and the crystalline mixture was expected to produce charged particles upon sublimation due to the intrinsic vacuum at the inlet aperture of the miniature mass spectrometer.

4. The method for rapid on-site detection of fentanyl analogs using a miniature mass spectrometer according to claim 1, wherein: the base and height of the triangular paper substrate are 1 cm and 1.5 cm, respectively.