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Volumn 51, Issue 1, 2010, Pages 107-113

Quantitative determination of residual active pharmaceutical ingredients and intermediates on equipment surfaces by ion mobility spectrometry

Author keywords

Cleaning verification; Ion mobility spectrometry; Pharmaceutical analysis; Swab analysis

Indexed keywords

DRUG;

EID: 70349435267     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2009.08.016     Document Type: Article
Times cited : (24)

References (58)
  • 2
    • 70349418736 scopus 로고    scopus 로고
    • ICH Q7A, Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients, 2000.
    • ICH Q7A, Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients, 2000.
  • 3
    • 70349418738 scopus 로고    scopus 로고
    • PIC/S, Guide to Good Manufacturing Practice for Medicinal Products, PE009-9, 2009.
    • PIC/S, Guide to Good Manufacturing Practice for Medicinal Products, PE009-9, 2009.
  • 4
    • 70349418740 scopus 로고    scopus 로고
    • PIC/S, Recommendations on validation master plan, installation and operational qualification, non-sterile process validation, cleaning validation, PI 006-2, 2004.
    • PIC/S, Recommendations on validation master plan, installation and operational qualification, non-sterile process validation, cleaning validation, PI 006-2, 2004.
  • 6
    • 55849101110 scopus 로고    scopus 로고
    • Equipment cleaning validation: developing an HPLC method to determine contamination residues on equipment surfaces
    • Shabir G.A. Equipment cleaning validation: developing an HPLC method to determine contamination residues on equipment surfaces. Am. Pharm. Rev. 11 (2008) 16-22
    • (2008) Am. Pharm. Rev. , vol.11 , pp. 16-22
    • Shabir, G.A.1
  • 7
    • 55849102100 scopus 로고    scopus 로고
    • The application of PAT for cleaning and cleaning validation
    • Hellings M., and Vanbaelen H. The application of PAT for cleaning and cleaning validation. Am. Pharm. Rev. 11 (2008) 12-21
    • (2008) Am. Pharm. Rev. , vol.11 , pp. 12-21
    • Hellings, M.1    Vanbaelen, H.2
  • 8
    • 14644422155 scopus 로고    scopus 로고
    • A validated HPLC method for determining residues of a dual active ingredient anti-malarial drug on manufacturing equipment surfaces
    • Boca M.B., Apostolides Z., and Pretorius E. A validated HPLC method for determining residues of a dual active ingredient anti-malarial drug on manufacturing equipment surfaces. J. Phar. Biomed. Anal. 37 (2005) 461-468
    • (2005) J. Phar. Biomed. Anal. , vol.37 , pp. 461-468
    • Boca, M.B.1    Apostolides, Z.2    Pretorius, E.3
  • 9
    • 33645966245 scopus 로고    scopus 로고
    • Cleaning validation 1: development and validation of a chromatographic method for the detection of traces of LpHse detergent
    • Zayas J., Colon H., Garced O., and Ramos L.M. Cleaning validation 1: development and validation of a chromatographic method for the detection of traces of LpHse detergent. J. Pharm. Biomed. Anal. 41 (2006) 589-593
    • (2006) J. Pharm. Biomed. Anal. , vol.41 , pp. 589-593
    • Zayas, J.1    Colon, H.2    Garced, O.3    Ramos, L.M.4
  • 10
    • 34250644378 scopus 로고    scopus 로고
    • Quantitative determination and sampling of lamivudine and zidovudine residues for cleaning validation in a production area
    • Santoro M.I., Fazio T.T., Singh A.K., and Kedor-hackmann E.R. Quantitative determination and sampling of lamivudine and zidovudine residues for cleaning validation in a production area. J. AOAC Int. 90 (2007) 715-719
    • (2007) J. AOAC Int. , vol.90 , pp. 715-719
    • Santoro, M.I.1    Fazio, T.T.2    Singh, A.K.3    Kedor-hackmann, E.R.4
  • 11
    • 33847135774 scopus 로고    scopus 로고
    • Quantitative determination and sampling of azathioprine residues for cleaning validation in production area
    • Fazio T.T., Singh A.K., Kedor-hackmann E.R., and Santoro M.I. Quantitative determination and sampling of azathioprine residues for cleaning validation in production area. J. Phar. Biomed. Anal. 43 (2007) 1495-1498
    • (2007) J. Phar. Biomed. Anal. , vol.43 , pp. 1495-1498
    • Fazio, T.T.1    Singh, A.K.2    Kedor-hackmann, E.R.3    Santoro, M.I.4
  • 12
    • 34047249413 scopus 로고    scopus 로고
    • Cleaning validation 2: development and validation of an ion chromatographic method for the detection of traces of CIP-100 detergent
    • Resto W., Hernandez D., Rey R., Colon H., and Zayas J. Cleaning validation 2: development and validation of an ion chromatographic method for the detection of traces of CIP-100 detergent. J. Pharm. Biomed. Anal. 44 (2007) 265-269
    • (2007) J. Pharm. Biomed. Anal. , vol.44 , pp. 265-269
    • Resto, W.1    Hernandez, D.2    Rey, R.3    Colon, H.4    Zayas, J.5
  • 13
    • 33847101483 scopus 로고    scopus 로고
    • Cleaning verification assays for highly potent compounds by high performance liquid chromatography mass spectrometry: strategy, validation, and long-term performance
    • Liu L., and Pack B.W. Cleaning verification assays for highly potent compounds by high performance liquid chromatography mass spectrometry: strategy, validation, and long-term performance. J. Pharm. Biomed. Anal. 43 (2006) 1206-1212
    • (2006) J. Pharm. Biomed. Anal. , vol.43 , pp. 1206-1212
    • Liu, L.1    Pack, B.W.2
  • 14
    • 33750362062 scopus 로고    scopus 로고
    • Validation of the total organic carbon (TOC) swab sampling and test method
    • Glover C. Validation of the total organic carbon (TOC) swab sampling and test method. PDA J. Pharm. Sci. Technol. 60 (2006) 284-290
    • (2006) PDA J. Pharm. Sci. Technol. , vol.60 , pp. 284-290
    • Glover, C.1
  • 15
    • 0038064325 scopus 로고    scopus 로고
    • Development and validation of a liquid chromatographic method for the determination of amlodipine residues on manufacturing equipment surfaces
    • Klinkenberg R., Streel B., and Ceccato A. Development and validation of a liquid chromatographic method for the determination of amlodipine residues on manufacturing equipment surfaces. J. Pharm. Biomed. Anal. 32 (2003) 345-352
    • (2003) J. Pharm. Biomed. Anal. , vol.32 , pp. 345-352
    • Klinkenberg, R.1    Streel, B.2    Ceccato, A.3
  • 16
    • 0037462526 scopus 로고    scopus 로고
    • Fast supercritical fluid extraction and high-resolution gas chromatography with electron-capture and flame photometric detection for multiresidue screening of organochlorine and organophosphorus pesticides in Brazil's medicinal plants
    • Zuin V.G., Yariwake J.H., and Bicchi C. Fast supercritical fluid extraction and high-resolution gas chromatography with electron-capture and flame photometric detection for multiresidue screening of organochlorine and organophosphorus pesticides in Brazil's medicinal plants. J. Chromatogr. A. 985 (2003) 159-166
    • (2003) J. Chromatogr. A. , vol.985 , pp. 159-166
    • Zuin, V.G.1    Yariwake, J.H.2    Bicchi, C.3
  • 17
    • 0037026372 scopus 로고    scopus 로고
    • Development and validation of an LC assay for sumatriptan succinate residues on surfaces in the manufacture of pharmaceuticals
    • Nozal M.J., Bernal J.L., Toribio L., Martin M.T., and Diez F.J. Development and validation of an LC assay for sumatriptan succinate residues on surfaces in the manufacture of pharmaceuticals. J. Pharm. Biomed. Anal. 30 (2002) 285-291
    • (2002) J. Pharm. Biomed. Anal. , vol.30 , pp. 285-291
    • Nozal, M.J.1    Bernal, J.L.2    Toribio, L.3    Martin, M.T.4    Diez, F.J.5
  • 18
    • 0034664090 scopus 로고    scopus 로고
    • Development and validation of an HPLC assay for fentanyl, alfentanil, and sufentanil in swab samples
    • Lambropoulos J., Spanos G.A., and Lazaridis N.V. Development and validation of an HPLC assay for fentanyl, alfentanil, and sufentanil in swab samples. J. Pharm. Biomed. Anal. 23 2-3 (2000) 421-428
    • (2000) J. Pharm. Biomed. Anal. , vol.23 , Issue.2-3 , pp. 421-428
    • Lambropoulos, J.1    Spanos, G.A.2    Lazaridis, N.V.3
  • 19
    • 0034073239 scopus 로고    scopus 로고
    • Low-level (PPB) determination of cisplatin in cleaning validation (rinse water) samples. I. An atomic absorption spectrophotometric method
    • Raghavan R., and Mulligan J.A. Low-level (PPB) determination of cisplatin in cleaning validation (rinse water) samples. I. An atomic absorption spectrophotometric method. Drug Dev. Ind. Pharm. 26 (2000) 423-428
    • (2000) Drug Dev. Ind. Pharm. , vol.26 , pp. 423-428
    • Raghavan, R.1    Mulligan, J.A.2
  • 20
    • 0034028373 scopus 로고    scopus 로고
    • Low-level (PPB) determination of cisplatin in cleaning validation (rinse water) samples. II. A high-performance liquid chromatographic method
    • Raghavan R., Burchett M., and Mulligan J.A. Low-level (PPB) determination of cisplatin in cleaning validation (rinse water) samples. II. A high-performance liquid chromatographic method. Drug Dev. Ind. Pharm. 26 (2000) 429-440
    • (2000) Drug Dev. Ind. Pharm. , vol.26 , pp. 429-440
    • Raghavan, R.1    Burchett, M.2    Mulligan, J.A.3
  • 21
    • 0033978105 scopus 로고    scopus 로고
    • Validation of the removal of acetylsalicylic acid. Recovery and determination of residues on various surfaces by high performance liquid chromatography
    • Nozal M.J., Bernal J.L., Toribio L., Jimenez J.J., and Martin M.T. Validation of the removal of acetylsalicylic acid. Recovery and determination of residues on various surfaces by high performance liquid chromatography. J. Chromatogr. A. 870 (2000) 69-75
    • (2000) J. Chromatogr. A. , vol.870 , pp. 69-75
    • Nozal, M.J.1    Bernal, J.L.2    Toribio, L.3    Jimenez, J.J.4    Martin, M.T.5
  • 22
    • 0032006070 scopus 로고    scopus 로고
    • Capillary gas chromatographic assay of residual methenamine hippurate in equipment cleaning validation swabs
    • Mirza T., George R.C., Bodenmiller J.R., and Belanich S.A. Capillary gas chromatographic assay of residual methenamine hippurate in equipment cleaning validation swabs. J. Pharm. Biomed. Anal. 16 (1998) 939-950
    • (1998) J. Pharm. Biomed. Anal. , vol.16 , pp. 939-950
    • Mirza, T.1    George, R.C.2    Bodenmiller, J.R.3    Belanich, S.A.4
  • 23
    • 0031431776 scopus 로고    scopus 로고
    • Total organic carbon method for aspirin cleaning validation
    • Holmes A.J., and Vanderwielen A.J. Total organic carbon method for aspirin cleaning validation. PDA J. Pharm. Sci. Technol. 51 (1997) 149-152
    • (1997) PDA J. Pharm. Sci. Technol. , vol.51 , pp. 149-152
    • Holmes, A.J.1    Vanderwielen, A.J.2
  • 24
    • 33744469089 scopus 로고    scopus 로고
    • Cleaning validation of multiproduct facility for liquid pharmaceutical forms: zidovudine syrup case
    • De Alencar J.R., Jimenez R.C., Santos R., Ramos S.V., and Neto P.J. Cleaning validation of multiproduct facility for liquid pharmaceutical forms: zidovudine syrup case. Acta Farmaceutica Bonaerense 25 (2006) 35-42
    • (2006) Acta Farmaceutica Bonaerense , vol.25 , pp. 35-42
    • De Alencar, J.R.1    Jimenez, R.C.2    Santos, R.3    Ramos, S.V.4    Neto, P.J.5
  • 25
    • 4043175552 scopus 로고    scopus 로고
    • Cleaning validation of zidovudine: strategy applied to the process manufacture of antiretroviral medicines
    • De Alencar J.R., Ramos S.V., Machado L.B., Oliveira A.T., and Neto P.J. Cleaning validation of zidovudine: strategy applied to the process manufacture of antiretroviral medicines. Brazilian J. Pharm. Sci. 40 (2004) 1-8
    • (2004) Brazilian J. Pharm. Sci. , vol.40 , pp. 1-8
    • De Alencar, J.R.1    Ramos, S.V.2    Machado, L.B.3    Oliveira, A.T.4    Neto, P.J.5
  • 26
    • 0036380514 scopus 로고    scopus 로고
    • Methods for the determination of detection limits for herbal mother tinctures on high-grade steel surfaces
    • Wollenweber C., Baier H.R., Adali M., Bulic M., and Koetting J. Methods for the determination of detection limits for herbal mother tinctures on high-grade steel surfaces. Pharmazeutische Industrie 64 (2002) 816-821
    • (2002) Pharmazeutische Industrie , vol.64 , pp. 816-821
    • Wollenweber, C.1    Baier, H.R.2    Adali, M.3    Bulic, M.4    Koetting, J.5
  • 27
    • 0033933250 scopus 로고    scopus 로고
    • Differentiating Organic carbon analysis for characterization of purified water and identification and quantification of residues in aqueous rinses from cleaning validation
    • Woiwode W., and Huber S. Differentiating Organic carbon analysis for characterization of purified water and identification and quantification of residues in aqueous rinses from cleaning validation. Pharmazeutische Industrie 62 (2000) 377-381
    • (2000) Pharmazeutische Industrie , vol.62 , pp. 377-381
    • Woiwode, W.1    Huber, S.2
  • 28
    • 0033120887 scopus 로고    scopus 로고
    • Cleaning level acceptance criteria and a high pressure liquid chromatography procedure for the assay of meclizine hydrochloride residue in swabs collected from pharmaceutical manufacturing equipment surfaces
    • Mirza T., Lunn M.J., Keeley F.J., George R.C., and Bodenmiller J.R. Cleaning level acceptance criteria and a high pressure liquid chromatography procedure for the assay of meclizine hydrochloride residue in swabs collected from pharmaceutical manufacturing equipment surfaces. J. Pharm. Biomed. Anal. 19 (1999) 747-756
    • (1999) J. Pharm. Biomed. Anal. , vol.19 , pp. 747-756
    • Mirza, T.1    Lunn, M.J.2    Keeley, F.J.3    George, R.C.4    Bodenmiller, J.R.5
  • 29
    • 0025744047 scopus 로고
    • Determination of clarithromycin as a contaminant on surfaces by high performance liquid chromatography using electrochemical detection
    • Rotsch T.D., Spanton M., Cugier P., and Plasz A.C. Determination of clarithromycin as a contaminant on surfaces by high performance liquid chromatography using electrochemical detection. Pharm. Res. 8 (1991) 989-991
    • (1991) Pharm. Res. , vol.8 , pp. 989-991
    • Rotsch, T.D.1    Spanton, M.2    Cugier, P.3    Plasz, A.C.4
  • 30
    • 70349428978 scopus 로고    scopus 로고
    • Validation of an HPLC method for analysis of nifedipine residues on stainless-steel surfaces in the manufacture of pharmaceuticals
    • Milenović D.M., Lazić M.L., Veljković V.B., and Todorović Z.B. Validation of an HPLC method for analysis of nifedipine residues on stainless-steel surfaces in the manufacture of pharmaceuticals. Acta Chromatographica 20 (2008) 183-194
    • (2008) Acta Chromatographica , vol.20 , pp. 183-194
    • Milenović, D.M.1    Lazić, M.L.2    Veljković, V.B.3    Todorović, Z.B.4
  • 31
    • 70349412163 scopus 로고    scopus 로고
    • The use of ion chromatography for the determination of clean-in-place-200 (CIP-200) detergent traces
    • Resto W., Roque J., Rey R., Colon H., and Zayas J. The use of ion chromatography for the determination of clean-in-place-200 (CIP-200) detergent traces. Anal. Chem. Insights 1 (2006) 5-12
    • (2006) Anal. Chem. Insights , vol.1 , pp. 5-12
    • Resto, W.1    Roque, J.2    Rey, R.3    Colon, H.4    Zayas, J.5
  • 32
    • 27644589616 scopus 로고    scopus 로고
    • Development and Validation of a thin-layer chromatographic method for determination of chloramphenicol residues on pharmaceutical equipment surfaces
    • Vovk I., and Simonovska B. Development and Validation of a thin-layer chromatographic method for determination of chloramphenicol residues on pharmaceutical equipment surfaces. J. AOAC Int.s 88 (2005) 1555-1561
    • (2005) J. AOAC Int.s , vol.88 , pp. 1555-1561
    • Vovk, I.1    Simonovska, B.2
  • 33
    • 35148853663 scopus 로고    scopus 로고
    • HPLC with charged aerosol detection for pharmaceutical cleaning validation
    • Forsatz B., and Snow N.H. HPLC with charged aerosol detection for pharmaceutical cleaning validation. LCGC North Am. 25 (2007) 960-968
    • (2007) LCGC North Am. , vol.25 , pp. 960-968
    • Forsatz, B.1    Snow, N.H.2
  • 35
    • 39149137215 scopus 로고    scopus 로고
    • Assessment of MEKC suitability for residue drug monitoring on pharmaceutical manufacturing equipment
    • Boca M.B., Pretorius E., Kgaje C., and Apostolides Z. Assessment of MEKC suitability for residue drug monitoring on pharmaceutical manufacturing equipment. J. Pharm. Biomed. Anal. 46 (2008) 631-638
    • (2008) J. Pharm. Biomed. Anal. , vol.46 , pp. 631-638
    • Boca, M.B.1    Pretorius, E.2    Kgaje, C.3    Apostolides, Z.4
  • 36
    • 0035102960 scopus 로고    scopus 로고
    • Ensuring successful validation: the logical steps to efficient cleaning procedures
    • Amer G., and Deshmane P. Ensuring successful validation: the logical steps to efficient cleaning procedures. BioPharm. 14 (2001) 26-32
    • (2001) BioPharm. , vol.14 , pp. 26-32
    • Amer, G.1    Deshmane, P.2
  • 37
    • 17644423442 scopus 로고    scopus 로고
    • Using visible residue limits for introducing new compounds into a pharmaceutical research facility
    • Forsyth R.J., and Van Nostrand V. Using visible residue limits for introducing new compounds into a pharmaceutical research facility. Pharm. Technol. 29 (2005) 134-140
    • (2005) Pharm. Technol. , vol.29 , pp. 134-140
    • Forsyth, R.J.1    Van Nostrand, V.2
  • 38
    • 33646702585 scopus 로고    scopus 로고
    • Enhancing drug development by applying LC-MS-MS for cleaning validation in manufacturing equipment
    • Kolodsick K.J., Phillips H., Feng J., Molski M., and Kingsmill C.A. Enhancing drug development by applying LC-MS-MS for cleaning validation in manufacturing equipment. Pharm. Technol. 30 (2006) 56-71
    • (2006) Pharm. Technol. , vol.30 , pp. 56-71
    • Kolodsick, K.J.1    Phillips, H.2    Feng, J.3    Molski, M.4    Kingsmill, C.A.5
  • 40
    • 33751519143 scopus 로고    scopus 로고
    • In situ spectroscopic cleaning validation
    • Urbas A.A., and Lodder R.A. In situ spectroscopic cleaning validation. NIR News 14 (2003) 8-10
    • (2003) NIR News , vol.14 , pp. 8-10
    • Urbas, A.A.1    Lodder, R.A.2
  • 42
    • 27544513935 scopus 로고    scopus 로고
    • Quantification of active pharmaceutical ingredients on metal surfaces using a Mid-IR grazing-angle fiber optics probe - an in situ cleaning verification process
    • Teelucksingh N., and Reddy K.B. Quantification of active pharmaceutical ingredients on metal surfaces using a Mid-IR grazing-angle fiber optics probe - an in situ cleaning verification process. Spectros. 20 (2005) 16-23
    • (2005) Spectros. , vol.20 , pp. 16-23
    • Teelucksingh, N.1    Reddy, K.B.2
  • 43
    • 55749094601 scopus 로고    scopus 로고
    • Cleaning validation - the rise of TOC
    • Bristol P. Cleaning validation - the rise of TOC. Manuf. Chem. 75 (2004) 37-38
    • (2004) Manuf. Chem. , vol.75 , pp. 37-38
    • Bristol, P.1
  • 44
    • 0036061651 scopus 로고    scopus 로고
    • Development of analytical methods to accurately and precisely determine residual active pharmaceutical ingredients and cleaning agents on pharmaceutical surfaces
    • Shifflet M.J., and Shapiro M. Development of analytical methods to accurately and precisely determine residual active pharmaceutical ingredients and cleaning agents on pharmaceutical surfaces. Am. Pharm. Rev. (2002) 35-40
    • (2002) Am. Pharm. Rev. , pp. 35-40
    • Shifflet, M.J.1    Shapiro, M.2
  • 45
    • 55849113896 scopus 로고    scopus 로고
    • Test method validation for cleaning validation samples
    • Forsyth R. Test method validation for cleaning validation samples. Eur. Pharm. Rev. 2 (2008)
    • (2008) Eur. Pharm. Rev. , vol.2
    • Forsyth, R.1
  • 47
    • 33745229895 scopus 로고    scopus 로고
    • Using ion mobility spectrometry for cleaning verification in pharmaceutical manufacturing
    • Walia G., Davis M., Stefanou S., and Debono R. Using ion mobility spectrometry for cleaning verification in pharmaceutical manufacturing. Pharm. Technol. April (2002) 72-78
    • (2002) Pharm. Technol. , vol.April , pp. 72-78
    • Walia, G.1    Davis, M.2    Stefanou, S.3    Debono, R.4
  • 49
    • 50649125389 scopus 로고    scopus 로고
    • Ion mobility spectrometry: A fast, sensitivite and robust HPLC alternative, Lab. Equip
    • R. Debono, Ion mobility spectrometry: a fast, sensitivite and robust HPLC alternative, Lab. Equip.: Appl. Chromatogr., (2002) 20-23.
    • (2002) Appl. Chromatogr , pp. 20-23
    • Debono, R.1
  • 51
    • 70349418735 scopus 로고    scopus 로고
    • R. Sandor, R. DeBono, Novel analytical approaches to solving pharmaceutical problems. AAPS NEWSMAGAZINE, February (2005) 16-17.
    • R. Sandor, R. DeBono, Novel analytical approaches to solving pharmaceutical problems. AAPS NEWSMAGAZINE, February (2005) 16-17.
  • 52
    • 33748937014 scopus 로고    scopus 로고
    • K. Chiarello-Ebner, Pursuing efficiency: new developments in cleaning technology, Pharm. Technol. March (2006).
    • K. Chiarello-Ebner, Pursuing efficiency: new developments in cleaning technology, Pharm. Technol. March (2006).
  • 53
    • 0036794237 scopus 로고    scopus 로고
    • IMS limit test improves cleaning verification and method development, Pharm. Technol. Eur
    • October
    • R. Munden, R. Everitt, R. Sandor, J. Carroll, R. Debono, IMS limit test improves cleaning verification and method development, Pharm. Technol. Eur., October (2002).
    • (2002)
    • Munden, R.1    Everitt, R.2    Sandor, R.3    Carroll, J.4    Debono, R.5
  • 54
    • 2942610490 scopus 로고    scopus 로고
    • New IMS sample injector facilitates cleaning validation
    • Laura B. New IMS sample injector facilitates cleaning validation. Pharm. Technol. 28 6 (2004) 18-20
    • (2004) Pharm. Technol. , vol.28 , Issue.6 , pp. 18-20
    • Laura, B.1
  • 55
    • 39249085107 scopus 로고    scopus 로고
    • Pharmaceutical applications of ion mobility spectrometry
    • O_Donnell R.M., Sun X., de P., and Harrington B. Pharmaceutical applications of ion mobility spectrometry. Trend. Anal. Chem. 27 1 (2008) 44-53
    • (2008) Trend. Anal. Chem. , vol.27 , Issue.1 , pp. 44-53
    • O'Donnell, R.M.1    Sun, X.2    de, P.3    Harrington, B.4
  • 56
    • 70349424890 scopus 로고    scopus 로고
    • Cleaning verification: method development and validation using ion mobility spectrometry
    • Galella E., Jennings S., Srikoti M., and Bonasso E. Cleaning verification: method development and validation using ion mobility spectrometry. Pharm. Technol. 33 (2009) 60-63
    • (2009) Pharm. Technol. , vol.33 , pp. 60-63
    • Galella, E.1    Jennings, S.2    Srikoti, M.3    Bonasso, E.4
  • 57
    • 24944482438 scopus 로고    scopus 로고
    • Determination of Parabens in pharmaceutical formulations by solid-phase microextraction-ion mobility spectrometry
    • Lokhnauth J., and Snow N. Determination of Parabens in pharmaceutical formulations by solid-phase microextraction-ion mobility spectrometry. Anal. Chem. 77 (2005) 5938-5946
    • (2005) Anal. Chem. , vol.77 , pp. 5938-5946
    • Lokhnauth, J.1    Snow, N.2


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