in vivo and in vitro bioavailability assessment of topical corticosteroid: applications in pharma...
TRANSCRIPT
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In Vivo and In Vitro Bioavailability Assessment of Topical Corticosteroid: Applications in Pharma Industry
Muhammad Qamar- uz- Zaman Assistant Professor,Department of Pharmacy, The Islamia University of Bahawalpur.
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Objectives:
Topical formulations
In vivo and In vitro methods used for topical
corticosteroids formulations (ointments & Creams).
Applications of these studies in Pharma industry.
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Topical Formulations?
• Prescribed to apply the drug on the skin surface
to get local or systemic therapeutic effects.
e.g: Ointments, Creams, Lotions, Transdermal
patches etc.
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Need of Bioavailability studies (Topical Corticosteroids)
Bioavailability leads to Bioequivalence studies
to rank the relative pharmacological activities
of the plethora of available commercial
corticosteroids.
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Skin Structure
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Human Skin (epidermis)
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Bioavailability studies
Two types of studies are:
In vitro
Modified Franz cell method
In vivo
Tape stripping method
Skin Blanching method
HPLC method
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Franz Cell
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Continued….. (Franz Cell)
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Test Procedure (Franz Cell)
Materials:Synthetic hydrophobic polyvinylidene difluoride
membrane (Durapore HVHP type, Millipore, Massachusetts)
Commercially available formulation of 0.05% betamethasone dipropionate (Ointment or Cream)
Modified Franz Cell
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Continued…..
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Continued…..
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Continued…. Precautions:• The hydrophobic membranes used in the drug release
experiments are presoaked 5 minutes in either isopropyl myristate (IPM) or a 40:60 mixture of PEG 400: water prior to mounting on the modified Franz Cell.
• Thorough contact between the membrane and the formulation is visually confirmed by viewing the underside of the membrane.
• 40:60 (v/v) PEG400:water is used as vehicle as compare to water or phosphate buffered saline (pH 7.4).
• The drug dose applied to the synthetic membrane is 0.28 mg of betamethasone dipropionate / cm2
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In Vivo Methods
Tape stripping method
Skin Blanching method
High Performance Liquid Chromatography
(HPLC) method
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Tape Stripping Human Skin
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Continued……
Tape Stripping Human Skin Method: This approach is based on the assumption
that effective cutaneous therapy requires partitioning of the topically applied drug from its vehicle formulation into the stratum corneum
The amount of drug partitioning into stratum corneum can be objectively assessed by tape stripping the same and chemically quantitating the amount of drug in the tape strips.
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Procedure:
0.05% betamethasone dipropionate is applied to the same human subject
forearm at the same time on the right and left forearms under occlusion for
24 hours.
160 mg dose is placed in a 1.2-cm diameter Hilltop chamber and affixed via
the supplied adhesive tape to a 1.13 cm2 surface area on the volar aspect of
the forearms. This dose, approximately 142 mg of formulation/ cm2
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Continued….
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Continued…. A maximum of 3 chambers, equally spaced 2cm apart,
are applied to each forearm for each study, at least 6 cm
above the wrist and 6 cm below the antecubital fossa to
minimize the disturbance of the drug treatment
throughout normal daily activity.
All experimental skin site are maintained under
occlusion for 24 hours.
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Continued… After 24 hours of treatment, the chamber is removed, and residual
formulation on the skin surface is gently removed with a Teflon spatula. (The
drug treated site is gently wiped with three dry cotton applicators and allowed
to air dry for 1-3 minutes).
Ten individual 0.6 cm diameter disks of tape are utilized to tape strip the
center of the 1.2 cm diameter drug treated skin site.
The sequential tape strips are combined and extracted in clean, labeled 1.5mL
polypropylene microcentrifuge tubes with 200 μL of acetonitrile.
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Continued…
The tubes are capped and vortexed for 1minute at high speed
and centrifuged at 5000 rpm for 5 minutes.
The supernatant is transferred into clean, labeled
microcentrifuge tubes, 20 μL is injected into HPLC .
A single extraction of the tape strips containing drug and stratum
corneum is sufficient to routinely recover > 90% of the drug.
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Continued… HPLC conditions:
• Retention time: 6.45 min
• Column: C18 reverse phase column
• Temperature: 25 centigrade
• Flow rate: 1.2 mL/min
• Mobile phase: acetonitrile: distilled water (65:35v/v)
• Detector: UV at 254 nm
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Continued….
Precautions: Assessment of the amount of drug could be extremely variable due to
the differences in the amount of stratum corneum removed.
One approach to normalize the drug content in the tape strips among
the individuals tested is to divide the drug content by the amount of
tissue removed, thus giving a drug concentration, milligram of drug per
milligram of stratum corneum.
The amount of stratum corneum removed with the tape stripping
method can be determined by weighing the tape strips before and after
tape stripping.
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Skin Blanching Assay
• Bioequivalence of topical corticosteroids from
commercial cream and ointment formulation is
currently assessed with Skin Blanching Assay.
• Assay is Subjective
• Skin blanching is monitored in the remaining drug
treated skin site after tape stripping.
• Skin blanching is score using 0-4 scale by a single
investigator at 1, 24, and 48 hours after drug removal.
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Continued…• The practicality has been enhanced by combining
the effects of time and skin blanching into a
composite skin blanching score.
• The skin blanching score that is utilized in
correlation study assumes that the greater the
amount of drug remaining in the skin over time,
the more prolonged is the pharmacological effect.
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Continued…• The skin blanching score is therefore calculated
additively using the time interval of observation
(hours) multiplied by the extent of skin blanching
at that time interval.
For example: an extent of skin blanching at 1, 24,
48 hours of +4, +3, and +1, respectively, produces
a score of 124: [(1) x (+4) + (24) x (+3) + (48) x (+1)]
= 124.
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Skin blanching Scoring SystemExtent of Skin Blanching Description
0 No blanching
1 Slight, diffuse blanching with indistinct outline
2 More Intense blanching with half of the treated site perimeter outline
3 Marked blanching with a distinct outline of the treated site
4 Extreme blanching with a distinct outline of the treated site
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Applications in Pharma Industry In developing generic product development
To meet the regulatory requirements.
Helpful tool to enhance the marketing and
promotion of medicines.
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Thank you