A TEST FOR CONCENTRATION OF ELECTROLYTES IN SWEAT IN CYSTIC FIBROSIS OF THE PANCREAS UTILIZING PILOCARPINE BY IONTOPHORESIS

Gibson, Lewis E., Cooke, Robert E.·1959·Pediatrics
DOI 10.1542/peds.23.3.545

Cited by (999)

Items 101–200 of 999

  1. Gut microbiota signatures in cystic fibrosis: Loss of host CFTR function drives the microbiota enterophenotype
    Pamela Vernocchi, Federica DEL CHIERICO, Alessandra Russo, Fabio Majo, Martina Rossitto, Mariacristina Valerio, Luca Casadei, Antonietta La Storia, Francesca De Filippis, Cristiano Rizzo et al. · 2018 · PLoS ONE
  2. Lung Disease Associated with the IVS8 5T Allele of the CFTR Gene
    Peadar G. Noone, C A Pue, Zhaoqing Zhou, Kenneth J. Friedman, Emma L. Wakeling, Muttiah Ganeshananthan, Richard H. Simon, Lawrence M. Silverman, Michael R. Knowles · 2000 · American Journal of Respiratory and Critical Care Medicine
  3. Nasal potential difference: a clinical diagnostic test for cystic fibrosis
    Eric W.F.W. Alton, D C Currie, R Logan-Sinclair · 1990 · European Respiratory Journal
  4. Proteomic Profiling of Sweat Exosome Suggests its Involvement in Skin Immunity
    Chang-Xian Wu, Zheng‐Fei Liu · 2017 · Journal of Investigative Dermatology
  5. Early determination of cystic fibrosis by electrochemical chloride quantification in sweat
    Javier Gonzalo‐Ruiz, Roser Mas, Carmen de Haro, Enric Cabruja, Rafael Camero, M. Asunción Alonso‐Lomillo, Francesc Xavier Muñoz · 2008 · Biosensors and Bioelectronics
  6. Delayed Puberty in Girls With Cystic Fibrosis Despite Good Clinical Status
    Marie Johannesson, Claes Gottlieb, Lena Hjelte · 1997 · PEDIATRICS
  7. Flexible Sweat Sensors: From Films to Textiles
    Dan Luo, Haibo Sun, Qianqian Li, Xin Niu, Yin He, Hao Liu · 2023 · ACS Sensors
  8. Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected
    Teresa Casals, L. Bassas, J. Ruiz-Romero · 1995 · Human Genetics
  9. Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene
    Thilo D�rk, Ulrich Wulbrand, Thomas Richter · 1991 · Human Genetics
  10. Nasal potential difference measurements in patients with atypical cystic fibrosis
    Michael A. Wilschanski, H. Famini, Nurith Strauss‐Liviatan, Joseph Rivlin, Hannah Blau, Haim Bibi, Lea Bentur, Yaakov Yahav, H. Springer, Mordechai Reuven Kramer et al. · 2001 · European Respiratory Journal
  11. The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis
    Michèle D. Bishop, Steven D. Freedman, Julian Zielenski, Najma N. Ahmed, Annie Dupuis, Sheelagh Martin, Lynda E. Ellis, Julie Shea, Isabel K. Hopper, Mary L. Corey et al. · 2005 · Human Genetics
  12. A Comparison of Peak Sputum Tobramycin Concentration in Patients With Cystic Fibrosis Using Jet and Ultrasonic Nebulizer Systems
    Jay D. Eisenberg, MARGARET SULLIVAN PEPE, MARGARET SULLIVAN PEPE · 1997 · CHEST Journal
  13. Clinical features, survival rate, and prognostic factors in young adults with cystic fibrosis
    Nancy Ν. Huang, Daniel V. Schidlow, Ted H. Szatrowski, Judy Palmer, Lourdes R. Laraya-Cuasay, William H. Yeung, Karen Ann Hardy, Lynn Quitell, Stanley B. Fiel · 1987 · The American Journal of Medicine
  14. Cystic Fibrosis Gene Mutation in Two Sisters with Mild Disease and Normal Sweat Electrolyte Levels
    Theresa V. Strong, Lisa S. Smit, Steven V. Turpin, Jeffery L. Cole, Catherine Tom Hon, D. Markiewicz, Thomas L. Petty, Michael W. Millar Craig, Edward C. Rosenow, Lap‐Chee Tsui et al. · 1991 · New England Journal of Medicine
  15. Nutritional status of infants with cystic fibrosis associated with early diagnosis and intervention
    MS Marcus, S Sondel, PM Farrell · 1991 · American Journal of Clinical Nutrition
  16. Progression of cystic fibrosis lung disease as a function of serum immunoglobulin G levels: A 5-year longitudinal study
    William B. Wheeler, Mary Williams, Wallace J. Matthews · 1984 · The Journal of Pediatrics
  17. Parameters for the Diagnosis and Management of Sinusitus
    Sheldon L. Spector, I L Bernstein, James T.C. Li, William E. Berger, Michael Kaliner, Diane E. Schuller, Joann Blessing-Moore, Mark S. Dykewicz, Stanley M. Fìneman, R E Lee et al. · 1998 · Journal of Allergy and Clinical Immunology
  18. EFFECT OF SWIMMING ON FORCED EXPIRATION AND SPUTUM CLEARANCE IN CYSTIC FIBROSIS
    M Zach, Barbara Purrer, Béatrice Oberwaldner · 1981 · The Lancet
  19. What are the pathways of iontophoretic current flow through mammalian skin?
    Christopher Cullander · 1992 · Advanced Drug Delivery Reviews
  20. The relevance of sweat testing for the diagnosis of cystic fibrosis in the genomic era.
    Avantika Mishra, Ronda F. Greaves, John Massie · 2005 · Europe PMC (PubMed Central)
  21. New insights on gastro-oesophageal reflux in cystic fibrosis by longitudinal follow up.
    Anne Malfroot, Isidoor Dab · 1991 · Archives of Disease in Childhood
  22. Animal Models in the Pathophysiology of Cystic Fibrosis
    Anna Semaniakou, Roger P. Croll, Valerie M. Chappe · 2019 · Frontiers in Pharmacology
  23. Brushed nasal epithelial cells are a surrogate for bronchial epithelial CFTR studies
    Brewington, John J., Filbrandt, Erin T., LaRosa, F.J., Moncivaiz, Jessica D., Ostmann, Alicia J., Strecker, Lauren M., Clancy, John P. · 2018 · JCI Insight
  24. Autonomic Abnormalities and Autoantibodies to Beta-Adrenergic Receptors
    Claire M. Fraser, J. Craig Venter, Michael Kaliner · 1981 · New England Journal of Medicine
  25. Anaesthesia and cystic fibrosis
    Timothy Simon Walsh, Chris Young · 1995 · Anaesthesia
  26. Long-term comparative trial of positive expiratory pressure versus oscillating positive expiratory pressure (flutter) physiotherapy in the treatment of cystic fibrosis
    P.Maggie McIlwaine, Lawrence T. K. Wong, Donlim Peacock · 2001 · The Journal of Pediatrics
  27. Pseudomonas Colonization in Cystic Fibrosis
    Lucas L. Kulczycki · 1978 · JAMA
  28. Functional modules, mutational load and human genetic disease
    Norann A. Zaghloul, Nicholas Katsanis · 2010 · Trends in Genetics
  29. Physical enhancement of dermatologic drug delivery: Iontophoresis and phonophoresis
    Daniel G. Kassan, Agnes M. Lynch, Matthew J. Stiller · 1996 · Journal of the American Academy of Dermatology
  30. Lung symptoms in pseudohypoaldosteronism type 1 are associated with deficiency of the α-subunit of the epithelial sodium channel
    Charlotta Schaedel, Lars Marthinsen, Ann‐Charlotte Kristoffersson, Ragnhild Kornfält, Karl Olof Nilsson, Bo Orlenius, Lars Holmberg · 1999 · The Journal of Pediatrics
  31. Evolution of CT findings in patients with cystic fibrosis.
    Thomas H. Helbich, Gertraud Heinz‐Peer, Dominik Fleischmann, Claudia Wojnarowski, Patrick Wunderbaldinger, S Huber, Irmgard Eichler, Christian Herold · 1999 · American Journal of Roentgenology
  32. Glucose tolerance in cystic fibrosis.
    Susanne Lanng, Birger Thorsteinsson, Gunna Erichsen · 1991 · Archives of Disease in Childhood
  33. Transdermal delivery by iontophoresis
    Swati Rawat, Sudha Vengurlekar, B Rakesh · 2008 · Indian Journal of Pharmaceutical Sciences
  34. Prospective controlled study of home and hospital therapy of cystic fibrosis pulmonary disease
    Mary Alice Donati, Ginny Guenette, Harvey S. Auerbach · 1987 · The Journal of Pediatrics
  35. Quality of Well-Being Before and After Antibiotic Treatment of Pulmonary Exacerbation in Patients with Cystic Fibrosis
    David M. Orenstein, Edward N. Pattishall, Patricia A. Nixon, Elizabeth A. Ross, Robert M. Kaplan · 1990 · CHEST Journal
  36. Wearable Potentiometric Chloride Sweat Sensor: The Critical Role of the Salt Bridge
    Choi, Dong-Hoon, Kim, Jin Seob, Cutting, Garry R., Searson, Peter C. · 2016 · Analytical Chemistry
  37. Increased prevalence of CFTR mutations and variants and decreased chloride secretion in primary sclerosing cholangitis
    Meredith M. Regan, Peter R. Durie, Julian Zielenski, Sunil G. Sheth, Julie C. Shea, Michèle D. Bishop, Sanjiv Chopra, Emily Malmberg, Carolyn Walker, Ryan Ricci et al. · 2003 · Human Genetics
  38. Correlation of forced oscillation technique in preschool children with cystic fibrosis with pulmonary inflammation
    S Brennan · 2005 · Thorax
  39. IDENTIFICATION OF LEUKOTRIENES D AND B IN SPUTUM FROM CYSTIC FIBROSIS PATIENTS
    Oliver Cromwell, Howard R. Morris, MargaretE. Hodson, Mark J. Walport, Graham W. Taylor, John C Batten, A. Barry Kay · 1981 · The Lancet
  40. MATERNAL RADIATION AND MONGOLISM
    William J. Schull, J.V. Neel · 1962 · The Lancet
  41. Wearable Sweat Sensors: Background and Current Trends
    Tolga Kaya, Gengchen Liu, Jenny Che-Ting Ho, Kumar Yelamarthi, Kevin Charles Miller, Jeffrey E. Edwards, Alicja B. Stannard · 2018 · Electroanalysis
  42. β-Adrenergic Sweat Secretion as a Diagnostic Test for Cystic Fibrosis
    Paul Quinton, Laura Molyneux, Wan Ip, Annie Dupuis, Julie Avolio, Elizabeth D. Tullis, Douglas J. Conrad, A. K. M. Shamsuddin, Peter R. Durie, Tanja Y. Gonska · 2012 · American Journal of Respiratory and Critical Care Medicine
  43. Frequency of Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations and 5T Allele in Patients With Allergic Bronchopulmonary Aspergillosis
    Éric Marchand, Luc Delaunois, Pierre Brancaleone, Olivier Vandenplas, Michel Mairesse, Christine Verellen‐Dumoulin, Jean‐François Rahier · 2001 · CHEST Journal
  44. Diagnosis and Treatment of Cystic Fibrosis
    Christian Koch, Niels Høiby · 2000 · Respiration
  45. A mutation in the cystic fibrosis transmembrane conductance regulator gene associated with elevated sweat chloride concentrations in the absence of cystic fibrosis
    John E. Mickle · 1998 · Human Molecular Genetics
  46. The irritable colon of childhood (chronicnonspecific diarrhea syndrome)
    Martin Davidson, R. Wasserman · 1966 · The Journal of Pediatrics
  47. Cystic fibrosis: physical exercise versus chest physiotherapy.
    M Zach, Béatrice Oberwaldner, Florin Häusler · 1982 · Archives of Disease in Childhood
  48. Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Allelic Variants Relate to Shifts in Faecal Microbiota of Cystic Fibrosis Patients
    Serena Schippa, Valerio Iebba, Floriana Santangelo, Antonella Gagliardi, Riccardo Valerio De Biase, Antonella Stamato, S. Bertasi, Marco Lucarelli, Maria Pia Conte, Serena Quattrucci · 2013 · PLoS ONE
  49. In Vivo Lipid Peroxidation and Platelet Activation in Cystic Fibrosis
    Giovanni Ciabattoni, Giovanni Davı̀, Mirella Collura, L. Iapichino, Francesca Pardo, Antonina Ganci, Rossana Romagnoli, Jacques Maclouf, Carlo Patrono · 2000 · American Journal of Respiratory and Critical Care Medicine
  50. Influence of abnormal Cl- impermeability on sweating in cystic fibrosis
    Jan Bijman, Paul Quinton · 1984 · American Journal of Physiology-Cell Physiology
  51. Alveolar macrophages and CC chemokines are increased in children with cystic fibrosis
    Sean R. Brennan, Peter David Sly, Catherine L. Gangell, Nina C. Sturges, Kaye Winfield, Matthew E. Wikström, S. Gard, John W. Upham · 2009 · European Respiratory Journal
  52. Comparison of Intrapulmonary Percussive Ventilation and Chest Physiotherapy
    JoAnne E. Natale, John Pfeifle, Douglas N. Homnick · 1994 · CHEST Journal
  53. IDENTIFICATION AND QUANTITATION OF PRECIPITINS AGAINST PSEUDOMONAS AERUGINOSA IN PATIENTS WITH CYSTIC FIBROSIS BY MEANS OF CROSSED IMMUNOELECTROPHORESIS WITH INTERMEDIATE GEL
    Niels Høiby, N. H. AXELSEN · 1973 · Acta Pathologica Microbiologica Scandinavica Section B Microbiology and Immunology
  54. Risk of Pancreatitis with Mutation of the Cystic Fibrosis Gene
    C P Choudari, Thomas F. Imperiale, Stuart Sherman · 2004 · The American Journal of Gastroenterology
  55. Risk factors for initial acquisition of Pseudomonas aeruginosa in children with cystic fibrosis identified by newborn screening
    Judith H. Maselli, Marci K. Sontag, Jill M. Norris · 2003 · Pediatric Pulmonology
  56. Intron-8 polythymidine sequence in Australasian individuals with CF mutations R117H and R117C
    John Massie, Nicola Kazia Poplawski, Bridget M Wilcken · 2001 · European Respiratory Journal
  57. Bronchodilators Increase Airway Instability in Cystic Fibrosis
    Maximilian S. Zach, Béatrice Oberwaldner, Günter Forche · 1985 · American Review of Respiratory Disease
  58. Diagnosis of Cystic Fibrosis by Sweat Testing: Age-Specific Reference Intervals
    Avantika Mishra, Ronda F. Greaves, Katherine Helen Smith · 2008 · The Journal of Pediatrics
  59. Bronchiectasis in adult patients: an expression of heterozygosity for CFTR gene mutations?
    Teresa Casals, Javier de Gracia, Miguel Ángel Martínez Gallego · 2004 · Clinical Genetics
  60. Identification of a splice site mutation (2789+5 G>A) associated with small amounts of normal CFTRmRNA and mild cystic fibrosis
    William Edward Highsmith, Lauranell H. Burch, Zhaoqing Zhou, John C. Olsen, Theresa V. Strong, Terry Smith, Kenneth J. Friedman, Lawrence M. Silverman, Richard C. Boucher, Francis S. Collins et al. · 1997 · Human Mutation
  61. Effect of linoleic acid intake on growth of infants with cystic fibrosis
    AW van Egmond, MR Kosorok, Rebecca E. Koscik · 1996 · American Journal of Clinical Nutrition
  62. Neonatal screening for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis: four years' experience
    Enzo Ranieri, Barry D. Lewis, R L Gerace · 1994 · BMJ
  63. PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patients
    Marcho Chiarini, Cristiano Sabelli, Paola Melotti, Cecília Garlanda, Gianfranco Savoldi, Cinzia Mazza, Rita Padoan, Alessandro Plebani, Alberto Mantovani, Luigi Daniele Notarangelo et al. · 2010 · Genes and Immunity
  64. Hyperkalemia, hypertension and systemic acidosis without renal failure associated with a tubular defect in potassium excretion
    J.E. Arnold, John K. Healy · 1969 · The American Journal of Medicine
  65. Resting Energy Expenditure
    Hillel Naon, Shirley L. Hack, Michael T. Shelton, Richard C. Gotthoffer, David Gozal · 1993 · CHEST Journal
  66. The response of the sweat glands of the new‐born baby to thermal stimuli and to intradermal acetylcholine
    Kelly Foster, Edmund N Hey, G. Katz · 1969 · The Journal of Physiology
  67. THE ULTRASTRUCTURE AND HISTOPHYSIOLOGY OF HUMAN ECCRINE SWEAT GLANDS
    Bryce L. Munger · 1961 · The Journal of Cell Biology
  68. (D) Routes of delivery: Case studies
    Christopher Cullander, Richard H. Guy · 1992 · Advanced Drug Delivery Reviews
  69. Genotype Analysis for ΔF508, G551d and R553x Mutations in Children and Young Adults With Cystic Fibrosis With and Without Chronic Liver Disease
    Ann Duthie, Derek G. Doherty, Carolyn Williams · 1992 · Hepatology
  70. Eccrine Sweat as a Biofluid for Profiling Immune Biomarkers
    Katchman, Benjamin A., Zhu, Meilin, Blain Christen, Jennifer, Anderson, Karen S. · 2018 · PROTEOMICS – Clinical Applications
  71. A wearable potentiometric sensor with integrated salt bridge for sweat chloride measurement
    Dong‐Hoon Choi, Yi Li, Garry R. Cutting, Peter C. Searson · 2017 · Sensors and Actuators B Chemical
  72. Is cystic fibrosis a TH17 disease?
    Patricia J. Dubin, Florencia M. McAllister, Jay K. Kolls · 2007 · Inflammation Research
  73. The cystic fibrosis lower airways microbial metagenome
    Patricia Morán Losada, Philippe Chouvarine, Marie Dorda, Silke Hedtfeld, Samira Mielke, Angela Schulz, Lutz Wiehlmann, Burkhard Tümmler · 2016 · ERJ Open Research
  74. Sources of Variation in Sweat Chloride Measurements in Cystic Fibrosis
    Joseph Michael Collaco, Scott M. Blackman, Karen S. Raraigh, Harriet Corvol, Johanna M. Rommens, Rhonda G. Pace, Pierre‐Yves Boëlle, John McGready, Patrick R. Sosnay, Lisa J. Strug et al. · 2016 · American Journal of Respiratory and Critical Care Medicine
  75. Isoenzyme Studies in Transient Hyperphosphatasemia of Infancy
    Jerome R. Kraut · 1985 · American journal of diseases of children
  76. Newborn screening for cystic fibrosis in Victoria: 10 years' experience (1989‐1998)
    John Massie, Judith A. Glazner, COLIN F. ROBERTSON, Margaret Olsen, Ivan Francis · 2000 · The Medical Journal of Australia
  77. Gastroesophageal reflux and unexplained chronic respiratory disease in infants and children
    Anne Malfroot, Yvan Vandenplas, Marleen H. Verlinden · 1987 · Pediatric Pulmonology
  78. Long term follow up of changes in FEV1 and treatment intensity during Pseudomonas aeruginosa colonisation in patients with cystic fibrosis
    Manfred Ballmann, P. Rabsch, Horst von der Hardt · 1998 · Thorax
  79. Device Drug Delivery to the Eye
    Murray L. Friedberg, Uwe Pleyer, Bartly J. Mondino · 1991 · Ophthalmology
  80. WHAT IS A CYSTIC FIBROSIS DIAGNOSIS?
    Beryl J. Rosenstein · 1998 · Clinics in Chest Medicine
  81. Intestinal malabsorption in childhood.
    C. M. Anderson · 1966 · Archives of Disease in Childhood
  82. Use of Electronic Noses for Diagnosis of Digestive and Respiratory Diseases through the Breath
    Carlos Sánchez, José Pedro Santos, Jesús Lozano · 2019 · Biosensors
  83. The European Cystic Fibrosis Society Patient Registry: valuable lessons learned on how to sustain a disease registry
    Laura Viviani, Anna Zolin, Anil Mehta, Hanne Vebert Olesen · 2014 · Orphanet Journal of Rare Diseases
  84. A novel computational and structural analysis of nsSNPs in CFTR gene
    C. George Priya Doss, Ramalingam Rajasekaran, Chinnappan Sudandiradoss, K. Ramanathan, Rituraj Purohit, Rao Sethumadhavan · 2008 · Genomic Medicine
  85. The Sweat Metabolome of Screen-Positive Cystic Fibrosis Infants: Revealing Mechanisms beyond Impaired Chloride Transport
    Adriana Nori de Macedo, Stellena Mathiaparanam, Lauren Brick, Katherine Keenan, Tanja Y. Gonska, Linda Pedder, Stephen Hill, Philip Britz‐McKibbin · 2017 · ACS Central Science
  86. Stratifying infants with cystic fibrosis for disease severity using intestinal organoid swelling as a biomarker of CFTR function
    Karin M. de Winter‐de Groot, Hettie M. Janssens, Rick T. van Uum, Johanna F. Dekkers, Gitte Berkers, Annelotte M. Vonk, Evelien Kruisselbrink, Hugo Oppelaar, Robert G.J. Vries, Hans C. Clevers et al. · 2018 · European Respiratory Journal
  87. Recent Advances in Skin-Interfaced Wearable Sweat Sensors: Opportunities for Equitable Personalized Medicine and Global Health Diagnostics
    Kaylee M. Clark, Tyler R. Ray · 2023 · ACS Sensors
  88. Diagnosis of cystic fibrosis after newborn screening: The Australasian experience?twenty years and five million babies later: A consensus statement from the Australasian paediatric respiratory group
    John Massie, Barry S. Clements, and the Australian Paediatric Respiratory Group · 2005 · Pediatric Pulmonology
  89. Management and Survival of Meconium Ileus A 30-year Review
    Christina A. Del Pin, Christina Czyrko, Moritz M. Ziegler · 1992 · Annals of Surgery
  90. Immunoreactive trypsinogen screening for cystic fibrosis: Characterization of infants with a false‐positive screening test
    Michael J. Rock, Elaine H. Mischler, Philip M. Farrell · 1989 · Pediatric Pulmonology
  91. A placebo-controlled trial of cephalexin therapy in the ambulatory management of patients with cystic fibrosis
    Vera A Loening-Baucke, Elaine H. Mischler, Martin G. Myers · 1979 · The Journal of Pediatrics
  92. Normal Sweat Chloride Values Do Not Exclude the Diagnosis of Cystic Fibrosis
    Pier Franco Pignatti, Maurizio Luisetti · 1995 · American Journal of Respiratory and Critical Care Medicine
  93. Working Up a Good Sweat - The Challenges of Standardising Sweat Collection for Metabolomics Analysis.
    2017 · PubMed Central
  94. Transdermal and Intravenous Nano Drug Delivery Systems
    Monica Sharma · 2018 · Elsevier eBooks
  95. Five years of experience with biochemical cystic fibrosis newborn screening based on IRT/PAP in Germany
    Olaf Sommerburg, Jutta Hammermann, Martin S. Lindner et al. · 2015 · Pediatric Pulmonology
  96. Wearable microfluidic-based e-skin sweat sensors
    Humairah Tabasum, Nikita K. Gill, Rahul Mishra, Saifullah Lone · 2022 · RSC Advances
  97. Optimization study for metabolomics analysis of human sweat by liquid chromatography–tandem mass spectrometry in high resolution mode
    M. Calderón-Santiago, Feliciano Priego‐Capote, Bernabé Jurado Gámez, M. D. Luque de Castro · 2014 · Journal of Chromatography A
  98. Neonatal screening strategy for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis.
    Enzo Ranieri, Richard G Ryall, Charles Phillip Morris · 1991 · BMJ
  99. Occurrence and Timing of Childhood Overweight and Mortality: Findings from the Third Harvard Growth Study
    Aviva Must, Sarah M. Phillips, Elena N. Naumova · 2011 · The Journal of Pediatrics
  100. Iontophoretic (Transdermal) Delivery of Drugs: Overview of Historical Development
    Yie Wen Chien, Ajay K. Banga · 1989 · Journal of Pharmaceutical Sciences