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A Review Article of
              Xanthan Gum

  • Prepared by :           • Guided By :
    Mr. Hardik U. Patel        Mr. Nishant Upadhyay
    M.Pharm (2ndSEM)           Asst. Professor,
                               BMCP, SURAT.
    Bhagwan Mahavir
    College of Pharmacy,
    SURAT.
04/18/12                   JOURNAL CLUB               1
Content
•   Introduction
•   Review of Literature
•   Conclusion
•   References




04/18/12               JOURNAL CLUB   2
Introduction
•   1. Nonproprietary Names
•   BP: Xanthan gum
•   PhEur: Xanthani gummi
•   USPNF: Xanthan gum

• 2. Synonyms
• Corn sugar gum; E415; Keltrol; polysaccharide B-1459;
• Rhodigel; Vanzan NF; Xantural.



04/18/12                   JOURNAL CLUB                   3
………………Introduction



• 3. Molecular Formula : (C35H49O29)n



• 4. Molecular weight : 2×106
       The USPNF 23 describes xanthan gum as a high
  molecular weight polysaccharide gum. It contains D-glucose
  and D-mannose as the dominant hexose units, along with D-
  glucuronic acid and is prepared as the sodium, potassium, or
  calcium salt.


04/18/12                   JOURNAL CLUB                      4
Chemical Structure




04/18/12          JOURNAL CLUB   5
………………Introduction
• 6. Functional Category :
   – Stabilizing Agent,
   – Suspending Agent,
   – Viscosity increasing agent (1%).
• 7. Applications in Pharmaceutical Formulation
  or Technology :
•        Xanthan gum is widely used in oral and topical
  pharmaceutical formulations, cosmetics, and foods as a
  suspending and stabilizing agent.
• It is also used as a thickening and emulsifying agent. It is
  nontoxic, compatible with most other pharmaceutical
  ingredients, and has good stability and viscosity properties
  over a wide pH and temperature range.
04/18/12                    JOURNAL CLUB                         6
…………Introduction
• Xanthan gum has been incorporated in an ophthalmic liquid
  dosage form, which interacts with mucin, thereby helping in
  the prolonged retention of the dosage form in the precorneal
  area.
• Xanthan gum can also be used as an Excipients for spray-
  drying and freeze-drying processes for better results.
• Xanthan gum can be used to increase the bioadhesive
  strength in vaginal formulations and as a binder in colon
  specific drug delivery systems.
• Xanthan gum is also used as a hydrocolloid in the food
  industry, and in cosmetics it has been used as a thickening
  agent in shampoo.


04/18/12                   JOURNAL CLUB                          7
………Introduction

• 8. Description :
  Xanthan gum occurs as a cream- or white-coloured, odorless,
  free-flowing, fine powder.
• 9. Typical Properties :
• Acidity/alkalinity: pH = 6.0–8.0 for a 1% w/v aqueous solution.
• Freezing point: 0* c for a 1% w/v aqueous solution.
• Melting point: 270*c.
• Solubility: practically insoluble in ethanol and ether; soluble in
  cold or warm water.
• Viscosity (dynamic): 1200–1600 mPa s for a
  1% w/v aqueous solution at 25*c.


04/18/12                      JOURNAL CLUB                         8
……..Introduction
• 10. Stability and Storage Conditions :
• Xanthan gum is a stable material. Aqueous solutions are
  stable over a wide pH range (pH 3–12), although they
  demonstrate maximum stability at pH 4–10 and temperatures
  of 10–60*C.
• Xanthan gum solutions of less than 1% w/v concentration
  may be adversely affected by higher than ambient
  temperatures
• Solutions are also stable in the presence of enzymes, salts,
  acids, and bases.
• The bulk material should be stored in a well-closed container
  in a cool, dry place.


04/18/12                   JOURNAL CLUB                       9
………………..Introduction


• 11. Incompatibilities :
• Xanthan gum is an anionic material and is not usually
  compatible with cationic surfactants, polymers, or
  preservatives as precipitation occurs. Anionic and
  amphoteric surfactants at concentrations above 15% w/v
  cause precipitation of xanthan gum from a solution.
• Xanthan gum is compatible with most synthetic and natural
  viscosity-increasing agents. If it is to be combined with
  cellulose derivatives, then xanthan gum free of cellulase
  should be used to prevent depolymerization of the cellulose
  derivative.



04/18/12                   JOURNAL CLUB                         10
………………Introduction

• 12. Safety : Xanthan gum is widely used in oral and topical
  pharmaceutical formulations, cosmetics, and food products
  and is generally regarded as nontoxic and nonirritant at the
  levels employed as a pharmaceutical excipient.
• The estimated acceptable daily intake for xanthan gum has
  been set by the WHO at up to 10 mg/kg body-weight.




04/18/12                    JOURNAL CLUB                         11
Review Articles



04/18/12         JOURNAL CLUB   12
Xanthan–Alginate composite gel
                      Beads
• Bead Preparation : SA (1.5%, w/v) and XG (0.3, 0.5 and 1.0%,
  w/v) were dispersed in distilled water. XG–SA dispersion (80
  ml) was dropped through a 1.2mm inner diameter needle,
  from hypodermic syringe into 0.45M calcium chloride
  solution (200 ml).
• These beads were cured , filtered and rinsed with distilled
  water. Then dried at room temperature for 48hrs.
• To prepare the DCA beads, DS (1%, w/v) was added into the
  dispersion and completely dissolved with a homogenizer for
  5 min before cross-linking process, and then the preparation
  was proceeded as described above.

04/18/12                   JOURNAL CLUB                          13
Effect of XG on rheology and viscosity of SA
                      dispersion




04/18/12                JOURNAL CLUB                14
• It can be seen that relationship between shear rate and shear
  stress of SA and XG–SA dispersions showed a straight line,
  whereas non-linear curve of 0.3% and 0.5%XG dispersions
  was found.
• Incorporation of XG did not affect the flow behavior of SA
  dispersion.
• Viscosity coefficient of SA dispersion increased significantly
  with increasing amount of XG.




04/18/12                    JOURNAL CLUB                      15
Water uptake of the composite DCA beads(In Phosphate
              buffer & Distilled Water)




04/18/12               JOURNAL CLUB               16
DS release profile of DCA beads with different % of
        XG(In Phosphate buffer & Distilled Water)




04/18/12                 JOURNAL CLUB                    17
Conclusion
• Incorporation of XG into the DCA beads caused a change in matrix
  structure of the beads due to intermolecular hydrogen bonding
  between XG and SA, and formation of small aggregates of XG after
  dispersing into SA dispersion. The XG–DCA beads gave higher
  entrapment efficiency of DS and increased water uptake and swelling in
  pH 6.8 phosphate buffer and distilled water.
• In contrast, the 0.3%XG–DCA beads could retard the drug release in
  distilled water. However , higher content of XG in the DCA beads
  increased the release rate of DS. This was due to erosion of small
  aggregates of XG on the surface of the DCA beads. This finding
  suggested that XG could modulate physicochemical properties and drug
  release of the DCA beads, which based on the existence of molecular
  interaction of XG and SA.


   04/18/12                     JOURNAL CLUB                       18
Referance
• Xanthan–alginate composite gel beads: Molecular interaction
  and in vitro characterization.
  (International Journal of Pharmaceutics 331 (2007) 61–71)
• Handbook of Pharmaceutical Excipients. (Page: 821-823)
• :
  http://www.livestrong.com/article/315249-xanthan-gum/#ixzz1r9d
• www.Sciencedirect.com
• http://en.wikipedia.org/wiki/xanthan_gum




04/18/12                  JOURNAL CLUB                    19
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Xanthan gum2003

  • 1. A Review Article of Xanthan Gum • Prepared by : • Guided By : Mr. Hardik U. Patel Mr. Nishant Upadhyay M.Pharm (2ndSEM) Asst. Professor, BMCP, SURAT. Bhagwan Mahavir College of Pharmacy, SURAT. 04/18/12 JOURNAL CLUB 1
  • 2. Content • Introduction • Review of Literature • Conclusion • References 04/18/12 JOURNAL CLUB 2
  • 3. Introduction • 1. Nonproprietary Names • BP: Xanthan gum • PhEur: Xanthani gummi • USPNF: Xanthan gum • 2. Synonyms • Corn sugar gum; E415; Keltrol; polysaccharide B-1459; • Rhodigel; Vanzan NF; Xantural. 04/18/12 JOURNAL CLUB 3
  • 4. ………………Introduction • 3. Molecular Formula : (C35H49O29)n • 4. Molecular weight : 2×106 The USPNF 23 describes xanthan gum as a high molecular weight polysaccharide gum. It contains D-glucose and D-mannose as the dominant hexose units, along with D- glucuronic acid and is prepared as the sodium, potassium, or calcium salt. 04/18/12 JOURNAL CLUB 4
  • 6. ………………Introduction • 6. Functional Category : – Stabilizing Agent, – Suspending Agent, – Viscosity increasing agent (1%). • 7. Applications in Pharmaceutical Formulation or Technology : • Xanthan gum is widely used in oral and topical pharmaceutical formulations, cosmetics, and foods as a suspending and stabilizing agent. • It is also used as a thickening and emulsifying agent. It is nontoxic, compatible with most other pharmaceutical ingredients, and has good stability and viscosity properties over a wide pH and temperature range. 04/18/12 JOURNAL CLUB 6
  • 7. …………Introduction • Xanthan gum has been incorporated in an ophthalmic liquid dosage form, which interacts with mucin, thereby helping in the prolonged retention of the dosage form in the precorneal area. • Xanthan gum can also be used as an Excipients for spray- drying and freeze-drying processes for better results. • Xanthan gum can be used to increase the bioadhesive strength in vaginal formulations and as a binder in colon specific drug delivery systems. • Xanthan gum is also used as a hydrocolloid in the food industry, and in cosmetics it has been used as a thickening agent in shampoo. 04/18/12 JOURNAL CLUB 7
  • 8. ………Introduction • 8. Description : Xanthan gum occurs as a cream- or white-coloured, odorless, free-flowing, fine powder. • 9. Typical Properties : • Acidity/alkalinity: pH = 6.0–8.0 for a 1% w/v aqueous solution. • Freezing point: 0* c for a 1% w/v aqueous solution. • Melting point: 270*c. • Solubility: practically insoluble in ethanol and ether; soluble in cold or warm water. • Viscosity (dynamic): 1200–1600 mPa s for a 1% w/v aqueous solution at 25*c. 04/18/12 JOURNAL CLUB 8
  • 9. ……..Introduction • 10. Stability and Storage Conditions : • Xanthan gum is a stable material. Aqueous solutions are stable over a wide pH range (pH 3–12), although they demonstrate maximum stability at pH 4–10 and temperatures of 10–60*C. • Xanthan gum solutions of less than 1% w/v concentration may be adversely affected by higher than ambient temperatures • Solutions are also stable in the presence of enzymes, salts, acids, and bases. • The bulk material should be stored in a well-closed container in a cool, dry place. 04/18/12 JOURNAL CLUB 9
  • 10. ………………..Introduction • 11. Incompatibilities : • Xanthan gum is an anionic material and is not usually compatible with cationic surfactants, polymers, or preservatives as precipitation occurs. Anionic and amphoteric surfactants at concentrations above 15% w/v cause precipitation of xanthan gum from a solution. • Xanthan gum is compatible with most synthetic and natural viscosity-increasing agents. If it is to be combined with cellulose derivatives, then xanthan gum free of cellulase should be used to prevent depolymerization of the cellulose derivative. 04/18/12 JOURNAL CLUB 10
  • 11. ………………Introduction • 12. Safety : Xanthan gum is widely used in oral and topical pharmaceutical formulations, cosmetics, and food products and is generally regarded as nontoxic and nonirritant at the levels employed as a pharmaceutical excipient. • The estimated acceptable daily intake for xanthan gum has been set by the WHO at up to 10 mg/kg body-weight. 04/18/12 JOURNAL CLUB 11
  • 12. Review Articles 04/18/12 JOURNAL CLUB 12
  • 13. Xanthan–Alginate composite gel Beads • Bead Preparation : SA (1.5%, w/v) and XG (0.3, 0.5 and 1.0%, w/v) were dispersed in distilled water. XG–SA dispersion (80 ml) was dropped through a 1.2mm inner diameter needle, from hypodermic syringe into 0.45M calcium chloride solution (200 ml). • These beads were cured , filtered and rinsed with distilled water. Then dried at room temperature for 48hrs. • To prepare the DCA beads, DS (1%, w/v) was added into the dispersion and completely dissolved with a homogenizer for 5 min before cross-linking process, and then the preparation was proceeded as described above. 04/18/12 JOURNAL CLUB 13
  • 14. Effect of XG on rheology and viscosity of SA dispersion 04/18/12 JOURNAL CLUB 14
  • 15. • It can be seen that relationship between shear rate and shear stress of SA and XG–SA dispersions showed a straight line, whereas non-linear curve of 0.3% and 0.5%XG dispersions was found. • Incorporation of XG did not affect the flow behavior of SA dispersion. • Viscosity coefficient of SA dispersion increased significantly with increasing amount of XG. 04/18/12 JOURNAL CLUB 15
  • 16. Water uptake of the composite DCA beads(In Phosphate buffer & Distilled Water) 04/18/12 JOURNAL CLUB 16
  • 17. DS release profile of DCA beads with different % of XG(In Phosphate buffer & Distilled Water) 04/18/12 JOURNAL CLUB 17
  • 18. Conclusion • Incorporation of XG into the DCA beads caused a change in matrix structure of the beads due to intermolecular hydrogen bonding between XG and SA, and formation of small aggregates of XG after dispersing into SA dispersion. The XG–DCA beads gave higher entrapment efficiency of DS and increased water uptake and swelling in pH 6.8 phosphate buffer and distilled water. • In contrast, the 0.3%XG–DCA beads could retard the drug release in distilled water. However , higher content of XG in the DCA beads increased the release rate of DS. This was due to erosion of small aggregates of XG on the surface of the DCA beads. This finding suggested that XG could modulate physicochemical properties and drug release of the DCA beads, which based on the existence of molecular interaction of XG and SA. 04/18/12 JOURNAL CLUB 18
  • 19. Referance • Xanthan–alginate composite gel beads: Molecular interaction and in vitro characterization. (International Journal of Pharmaceutics 331 (2007) 61–71) • Handbook of Pharmaceutical Excipients. (Page: 821-823) • : http://www.livestrong.com/article/315249-xanthan-gum/#ixzz1r9d • www.Sciencedirect.com • http://en.wikipedia.org/wiki/xanthan_gum 04/18/12 JOURNAL CLUB 19