Quick NMR Method For Identification And Estimation Of Components In Hand-Rub Formulations

Abstract

The present invention relates to a method based on proton NMR technique to differentiate genuine and spurious Hand-rub formulations. This method identifies and estimates all four components present in WHO-recommended Hand-rub formulations. Further, this method also identifies the presence of non-recommended/additional components present in WHO-recommended Hand-rub formulations. The method described in this invention utilizes experimental parameters and derived equations to quantify all four components in just fifteen minutes without using any organic solvents.

Claims

1) A method for identifying and quantifying components in a hand-rub formulation, the method comprising: a) analyzing and characterizing the components by determining position of hydrogen attached to different atoms in each component based on proton NMR technique to obtain chemical shift of hydrogen as ppm peak results, and b) quantifying the components using experimental parameters and solving equations with the results obtained in step a) to arrive at the weight % of each component, wherein weight % refers to the percentage by weight of each component in the hand-rub formulation.

2) The method as claimed in claim 1, wherein the components in the hand-rub formulation are an alcohol, a peroxide, glycerol, and water.

3) The method as claimed in claim 2, wherein the method comprises analyzing and characterizing an alcohol, analyzing and characterizing a peroxide, analyzing and characterizing glycerol, analyzing and characterizing water.

4) The method as claimed in claim 3, wherein the alcohol is ethanol or isopropanol.

5) The method as claimed in claim 3, wherein the peroxide is hydrogen peroxide.

6) The method as claimed in claim 4, wherein the chemical shift of —OCH— signal of secondary hydrogen at 4.0 ppm is used for quantification of isopropanol.

7) The method as claimed in claim 2, wherein the chemical shift of —OCH— peak at 3.76 ppm is used for quantification of glycerol.

8) The method as claimed in claim 5, wherein the chemical shift of —OH at 5.5 ppm is used for quantification of hydrogen peroxide.

9) The method as claimed in claim 2, wherein the chemical shift of —OH at 4.77 ppm is used quantification of water.

10) The method as claimed in claims 1, wherein the chemical shifts in the proton NMR at 3.0 ppm to 6.0 ppm corresponding to isopropanol, glycerol, water, and hydrogen peroxide are used for quantification.

11) The method as claimed in claim 4, wherein the weight % of each component in a hand-rub formulation based on isopropanol has been quantified by the equation IT=IP+IG+IW +IH, and wherein IT is total integral, IP is Ip×molecular weight of isopropanol, IG is Ig×molecular weight of glycerol, IW is Iw×molecular weight of water, IH is Ih×molecular weight of hydrogen peroxide, wherein Ip, Ig, Iw and Ih are “one proton integral intensity” of isopropanol, glycerol, water, and hydrogen peroxide and is calculated by corresponding integral intensity of proton NMR spectrum divided by number of protons of the group.

12) The method as claimed in claim 11, wherein, Ip is an integration of 4.0 ppm peak, Ig is an integration of 3.76 ppm peak, Iw is an integration of 4.77 ppm peak divided by two after subtraction of isopropanol and glycerol —OH contributing protons, Ih is an integration of 5.5 ppm peak divided by two.

13) The method as claimed in claim 11, wherein, weight % of Isopropanol=(IP/IT)×100, weight % of Glycerol=(IG/IT)×100, weight % of Water=(IW/IT)×100, weight % of hydrogen peroxide=(IH/IT)×100.

14) The method as claimed in claim 4, wherein the weight % of each component in a hand-rub formulation based on ethanol has been quantified by the equation IT=IE+IG+IW+IH, and wherein IE is Ie×molecular weight of ethanol, IG is Ig×molecular weight of glycerol, IW is Iw×molecular weight of water, IH is Ih×molecular weight of hydrogen peroxide, wherein Ie, Ig, Iw and Ih are “one proton integral intensity” of ethanol, glycerol, water, and hydrogen peroxide and is calculated by corresponding integral intensity of proton NMR spectrum divided by number of protons of that group.

15) The method as claimed in claim 14, wherein, Ie is an integration of 1.14 ppm peak divided by three, Ig is an integration of 3.8 to 3.4 ppm peak—Ie×two, Iw is an integration of 4.7 ppm peak divided by two after subtraction of ethanol and glycerol —OH contributing protons, Ih is an integration of 5.4 ppm peak divided by two.

16) The method as claimed in claim 14, wherein, weight % of Ethanol=(IE/IT)×100, weight % of Glycerol=(IG/IT)×100, weight % of Water=(IW/IT)×100, weight % of hydrogen peroxide=(IH/IT)×100.

17) The method as claimed in claim 1, wherein the method based on proton NMR comprises identification and quantification of all components in a hand sanitizer formulation and provides equations for quantification of components in a hand sanitizer formulation.

18) The method as claimed in claim 17, wherein the chemical shift of proton NMR spectrum of the hand sanitizer formulation used is in the range of 0.0 ppm to 10.0 ppm.

19) The method as claimed in claim 17, wherein the method based on proton NMR further comprises identification of methanol in a hand sanitizer formulation.

20) The method as claimed in claim 19, wherein a sharp singlet is observed at 3.3 ppm of —OCH.sub.3 for methanol.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0029] To further clarify advantages and aspects of the invention, a more particular description of the invention will be rendered by reference to specific embodiments thereof, which is illustrated in the appended drawing(s). It is appreciated that the drawing(s) of the present invention depicts only typical embodiments of the invention and are therefore not to be considered limiting of its scope.

[0030] FIG. 1: depicts the NMR spectrum of the four components.

DETAILED DESCRIPTION OF THE INVENTION

[0031] Those skilled in the art will be aware that the present disclosure is subject to variations 1H NMR spectrum of IPA based Sanitizer and modifications other than those specifically described. It is to be understood that the present disclosure includes all such variations and modifications. The disclosure also includes all such steps of the process, features of the product, referred to or indicated in this specification, individually or collectively, and any and all combinations of any or more of such steps or features.

[0032] The present disclosure is not to be limited in scope by the specific embodiments described herein, which are intended for the purposes of exemplification only. Functionally equivalent products and methods are clearly within the scope of the disclosure, as described herein.

[0033] The present invention provides a method related to the analysis of Hand-rub formulations. In particular, the invention relates to a method based on proton NMR technique i.e., 1H NMR. The invention also relates to the identification and estimation of the components in Hand-rub formulations. The method described in this invention utilizes experimental parameters and derived equations to quantify all four components in just fifteen minutes.

[0034] In one embodiment, the present invention provides a method for identifying and quantifying components in a hand-rub formulation, the method comprising: [0035] a) analyzing and characterizing the components by determining position of hydrogen attached to different atoms in each component based on proton NMR technique to obtain chemical shift of hydrogen as ppm peak results, [0036] b) quantifying the components using experimental parameters and solving equations with the results obtained in step a) to arrive at the weight % of each component,
wherein weight % refers to the percentage by weight of each component in the hand-rub formulation.

[0037] In one aspect of the invention, a method of analyzing a sample containing one or more components, which comprises alcohol, peroxide, glycerol, and water, is provided. In one embodiment, the method includes steps of analyzing and characterizing the alcohol, analyzing and characterizing the peroxide, analyzing and characterizing the glycerol, analyzing and characterizing water, and determining the identity and quantity of all the components of the hand-rub formulation i.e., the sample using the results obtained from one or more of the analysis steps. In another embodiment, the equation method comprises generating equations from the results obtained from one or more of the analysis steps and solving them.

[0038] In an embodiment, the method is based on proton NMR i.e., 1H NMR. A person skilled in the art will acknowledge that Proton NMR experiment is the most common NMR experiment which involves the study of the hydrogen nucleus when subjected to nuclear magnetic resonance. Being the most sensitive nucleus, proton NMR usually yields sharp signals. At a given radio frequency, each hydrogen atom will need a slightly different magnetic field applied to it to bring it into the resonance condition depending on what exactly it is attached to. Hence, the magnetic field required becomes a very useful guide to the hydrogen atoms environment in the molecule. In an embodiment, the chemical shift of proton NMR spectrum of hand sanitizer used is from 0.0 ppm to 10.0 ppm.

[0039] In one embodiment, the method provided includes determining the position of hydrogen attached to the different atoms in all the components. In one aspect of the invention, the position of hydrogen is secondary, if the alcohol in the sample is isopropanol and/or ethanol. In another embodiment, the chemical shift of —OCH— signal of secondary hydrogen of isopropanol at 4.0 ppm is used for quantification of isopropanol. In another aspect of the invention, if the alcohol is methanol, a sharp singlet is observed at 3.3 ppm of —OCH.sub.3.

[0040] In an embodiment, the appearance of two resolved peaks of glycerol occurs at 3.76 ppm and 3.62-3.50 ppm corresponding to the chemical shift of hydrogen in —OCH— and —OCH.sub.2—, respectively. In another embodiment, the chemical shift of —OCH— peak at 3.76 is used for quantification of glycerol content.

[0041] In an embodiment, the chemical shift of —OH at 5.5 ppm is used for quantification of hydrogen peroxide. In another embodiment, the chemical shift of —OH at 4.77 ppm is used quantification of water.

[0042] In an embodiment, the chemical shifts in the proton NMR at 3.0 ppm to 6.0 ppm corresponding to isopropanol, glycerol, water, and hydrogen peroxide are used for quantification. In another embodiment, the quantitative analysis was carried out using integral intensities obtained under each signal from proton NMR spectrum.

[0043] In an embodiment, for hand-rub formulation based on isopropanol, the percentage of each component by weight i.e., weight % has been estimated by following equation:

IT=IP+IG+IW+IH

[0044] where

[0045] IT is total integral

[0046] IP is Ip×molecular weight of isopropanol,

[0047] IG is Ig×molecular weight of glycerol,

[0048] IW is Iw×molecular weight of water,

[0049] IH si Ih×molecular weight of hydrogen peroxide,

[0050] and, Ip, Ig, Iw and Ih are “one proton integral intensity” of iso-propanol, glycerol, water and hydrogen peroxide. “One proton integral intensity” is calculated by corresponding integral intensity of proton NMR spectrum divided by number of protons of the group.

[0051] Ip is an integration of 4.0 ppm peak,

[0052] Ig is an integration of 3.76 ppm peak,

[0053] Iw is an integration of 4.77 ppm peak, divided by two after subtraction of isopropanol and glycerol —OH contributing protons,

[0054] Ih is integration of 5.5 ppm peak divided by two

[0055] and,

[0056] weight % of Isopropanol=(IP/IT)×100,

[0057] weight % of Glycerol=(IG/IT)×100,

[0058] weight % of Water=(IW/IT)×100,

[0059] weight % of hydrogen peroxide=(IH/IT)×100.

[0060] In another embodiment, for hand-rub formulation based on ethanol, the percentage of each component by weight i.e., weight % has been estimated by following equation:

IT=IE+IG+IW+IH

[0061] where

[0062] IE is Ie×molecular weight of ethanol,

[0063] IG is Ig×molecular weight of glycerol,

[0064] IW is Iw×molecular weight of water,

[0065] IH is Ih×molecular weight of hydrogen peroxide, and, Ie, Ig, Iw and Ih are “one proton integral intensity” of ethanol, glycerol, water, and hydrogen peroxide. “One proton integral intensity” is calculated by corresponding integral intensity of proton NMR spectrum divided by number of protons of that group.

[0066] Ie is an integration of 1.14 ppm peak divided by three,

[0067] Ig is an integration of 3.8 to 3.4 ppm peak—Ie×two,

[0068] Iw is an integration of 4.7 ppm peak, divided by two after subtraction of ethanol and glycerol —OH

[0069] contributing protons,

[0070] Ih is an integration of 5.4 ppm peak divided by two,

[0071] And,

[0072] weight % of Ethanol=(IE/IT)×100,

[0073] weight % of Glycerol=(IG/IT)×100,

[0074] weight % of Water=(IW/IT)×100,

[0075] weight % of hydrogen peroxide=(IH/IT)×100.

[0076] In an embodiment, the method based on proton NMR provides identification and estimation of all components in hand sanitizer formulations. In another embodiment, the method provides equations for estimation of components in hand sanitizer.

EXAMPLE

Example 1

[0077] WHO recommended Hand-rub Formulation with Formulation II having final composition (v/v) of 75% of Iso-propanol, 0.125% of Hydrogen peroxide, 1.45% of Glycerol and Sterile distilled or boiled cold water was prepared and analyzed by proton NMR method to identify all components present in the formulation by following characteristic peaks. Iso-propanol was identified by the chemical shift of —OCH— signal of secondary hydrogen at 4.0 ppm, the appearance of two resolved peaks of glycerol were observed at 3.76 ppm and 3.62 to 3.50 ppm corresponding to the chemical shift of hydrogen in —OCH— and —OCH.sub.2— respectively, the chemical shift of —OH was visible at 5.5 ppm of hydrogen peroxide, and the chemical shift of —OH at 4.77 ppm indicated the presence of water.

Example 2

[0078] Iso-propanol, glycerol, hydrogen peroxide, and water in a formulation prepared by other group (Fuel department) were quantified by derived equations using integration of their characteristics signals and it was found that 71.3%, 2.3%, 0.18%, 26.2% of Iso-propanol, Hydrogen peroxide, Glycerol, and water respectively was present against actual concentration values of 73.3%, 2.3%, 0.19% and 24.81% of Iso-propanol, Hydrogen peroxide, Glycerol, and water respectively given by the Automotive department formulator.

Example 3

[0079] Iso-propanol, glycerol, hydrogen peroxide, and water in a laboratory prepared blend 1 which was prepared by other group was quantified and concentration of Iso-propanol, Hydrogen peroxide, Glycerol, and water was found as 51.2%, 9.2%, 0.2%, 39.4% respectively against actual concentration values of 53.1%, 8.5%, 0.14% and 38.26% of Iso-propanol, Hydrogen peroxide, Glycerol, and water respectively given by formulator.

[0080] Concentration of Iso-propanol, glycerol, and water found in blend 2 was 61.2%, 6.2% and 32.6% against actual concentrations of 63.9%, 5.9% and 29.94% respectively in blend 2. Estimation of hydrogen peroxide (H.sub.2O.sub.2) was not possible in blend 2 due to high concentration of H.sub.2O.sub.2. At this concentration, the hydrogen peroxide and water peaks coalesce to form a single peak that is broadened. This phenomenon is attributed to the exchange of protons between water and hydrogen peroxide. As the concentration of hydrogen peroxide increases, the rate of proton exchange between water and hydrogen peroxide becomes significant, and as a result, a single broadened peak is observed.

Example 4

[0081] WHO recommended Hand-rub Formulation with Formulation I having final composition (wt/wt %) of 76.5% of ethanol, 0.20% of Hydrogen peroxide, 2.5% of Glycerol, and 20.8 of Sterile distilled or boiled cold water was prepared and concentration of Ethanol, Hydrogen peroxide, Glycerol, and water estimated by NMR method of the present invention was 75.4%, 0.18%, 2.4% and 23.02% respectively.

Example 5

[0082] A commercial hand sanitizer was analyzed and iso-propanol, glycerol and water were found at concentrations of 45.2%, 1.10%, and 52.0% respectively, while 1.7% of methanol which is a toxic chemical was observed. Five more commercial samples were analyzed by this method and the iso-propanol concentration was found to be below WHO recommended concentration for COVID-19 hand sanitizers.

TECHNICAL ADVANTAGES OF THE INVENTION

[0083] 1. Designed experiments and solvent system for separating all four components.

[0084] 2. No organic solvent or standard used in this method.

[0085] 3. Quick and less time taking (one sample in just fifteen minutes).

[0086] 4. Derived the equations for quantification.

[0087] 5. Able to identify the presence of non-recommended/additional components.