{"id":2800,"date":"2025-09-22T15:34:32","date_gmt":"2025-09-22T08:34:32","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=2800"},"modified":"2025-11-24T11:10:49","modified_gmt":"2025-11-24T04:10:49","slug":"alendronic-acid-tablets","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/alendronic-acid-tablets\/","title":{"rendered":"Alendronic Acid Tablets"},"content":{"rendered":"

(Ph. Eur. 11.6 update)<\/p>\n

Action and use<\/strong><\/p>\n

Bisphosphonate; treatment of osteoporosis.<\/p>\n

DEFINITION<\/h2>\n

Alendronic Acid Tablets contain Sodium Alendronate Trihydrate.<\/p>\n

The tablets comply with the requirements stated under Tablets and with the following requirements.<\/p>\n

Content of alendronic acid, C4<\/sub>H13<\/sub>NO7<\/sub>P2<\/sub><\/p>\n

95.0 to 105.0% of the stated amount.<\/p>\n

IDENTIFICATION<\/h2>\n

A. Carry out the method for thin-layer chromatography, Appendix III A, using the following solutions.<\/p>\n

(1) Mix a quantity of the powdered tablets containing the equivalent of 76 mg of alendronic acid with 50 mL of water for 30 minutes with the aid of ultrasound and occasional shaking, and filter.<\/p>\n

(2) 0.2% w\/v of sodium alendronate BPCRS.<\/p>\n

CHROMATOGRAPHIC CONDITIONS<\/p>\n

(a) Use as the coating cellulose.<\/p>\n

(b) Use the mobile phase as described below.<\/p>\n

(c) Apply 2 \u03bcL of each solution.<\/p>\n

(d) Develop the plate to 15 cm.<\/p>\n

(e) After removal of the plate, dry in a current of warm air, spray with ninhydrin solution, heat at 100\u00b0 to 105\u00b0 for 15 minutes and examine.<\/p>\n

MOBILE PHASE<\/p>\n

1 volume of 13.5M ammonia, 8 volumes of 2.5% v\/v trichloroacetic acid and 11 volumes of methanol.<\/p>\n

CONFIRMATION<\/p>\n

The principal spot in the chromatogram obtained with solution (1) corresponds in position and colour to that in the chromatogram obtained with solution (2).<\/p>\n

B. In the Assay, the principal peak in the chromatogram obtained with solution (1) has the same retention time as the principal peak in the chromatogram obtained with solution (2).<\/p>\n

TESTS<\/h2>\n

Dissolution<\/h3>\n

Comply with the dissolution test for tablets and capsules, Appendix XII B1.<\/p>\n

TEST CONDITIONS<\/p>\n

(a) Use Apparatus 2, rotating the paddle at 50 revolutions per minute.<\/p>\n

(b) Use 900 mL of water, at a temperature of 37\u00b0, as the medium.<\/p>\n

PROCEDURE<\/p>\n

Carry out the method for liquid chromatography, Appendix III D, using the following solutions.<\/p>\n

(1) After 45 minutes, withdraw a sample of the medium and filter (Whatman GF\/C is suitable). Use the filtered sample diluted with the dissolution medium, if necessary, to produce a solution expected to contain the equivalent of 0.00084% w\/v of alendronic acid.<\/p>\n

(2) 0.0011% w\/v of sodium alendronate BPCRS in water.<\/p>\n

CHROMATOGRAPHIC CONDITIONS<\/p>\n

(a) Use a stainless steel column (15 cm \u00d7 4.6 mm) packed with anion exchange resin (7 \u03bcm) (Allsep Anion is suitable).<\/p>\n

(b) Use isocratic elution and the mobile phase described below.<\/p>\n

(c) Use a flow rate of 1.2 mL per minute.<\/p>\n

(d) Use a column temperature of 35\u00b0.<\/p>\n

(e) Use a refractive index detector, maintained at 40\u00b0.<\/p>\n

(f) Inject 100 \u03bcL of each solution.<\/p>\n

MOBILE PHASE<\/p>\n

0.02% v\/v of formic acid, pH adjusted to 3.5 with 2M sodium hydroxide.<\/p>\n

DETERMINATION OF CONTENT<\/p>\n

Calculate the total content of C4<\/sub>H13<\/sub>NO7<\/sub>P2<\/sub> in the medium using the declared content of C4<\/sub>H12<\/sub>NNaO7<\/sub>P2<\/sub>
\nin sodium alendronate BPCRS. Each mg of C4<\/sub>H12<\/sub>NNaO7<\/sub>P2<\/sub> is equivalent to 0.9189 mg of C4<\/sub>H13<\/sub>NO7<\/sub>P2<\/sub><\/p>\n

LIMITS<\/p>\n

The amount of alendronic acid released is not less than 75% (Q) of the stated amount.<\/p>\n

Related substances<\/h3>\n

Carry out the method for liquid chromatography, Appendix III D, using the following solutions.<\/p>\n

Buffer solution Prepare a solution containing 0.294% w\/v of sodium citrate and 0.142% w\/v of anhydrous disodium hydrogen orthophosphate, adjusted to pH 8.0 using orthophosphoric acid and filter.<\/p>\n

Solution A 2.94% w\/v of sodium citrate in water.<\/p>\n

Solution B 1.91% w\/v of sodium borate in water.<\/p>\n

Solution C 0.02% w\/v of (9-fluorenyl)methyl chloroformate in acetonitrile. Prepare immediately before use.<\/p>\n

(1) Mix a quantity of the powdered tablets containing the equivalent of 23 mg of alendronic acid with solution A and make up to 50 mL with the same solvent. Mix and filter (Whatman GF\/C is suitable), discarding the first 5 mL of filtrate. To 5 mL of the filtrate in a screw cap centrifuge tube add 5 mL of solution B and 10 mL of solution C, shake for 1 minute and allow to stand at room temperature for 30 minutes, add 20 mL of dichloromethane and shake vigorously for 1 minute; centrifuge and use the aqueous layer.<\/p>\n

(2) To 5 mL of a 0.0003% w\/v solution of 4-aminobutanoic acid in solution A in a screw cap centrifuge tube, add 5 mL of solution B and 10 mL of solution C, shake for 45 seconds and allow to stand at room temperature for 30 minutes, add 20 mL of dichloromethane and shake vigorously for 1 minute, centrifuge and use the aqueous layer.<\/p>\n

(3) To 5 mL of a solution containing 0.06% w\/v of sodium alendronate BPCRS and 0.01% w\/v of 4-aminobutanoic acid in solution A in a screw cap centrifuge tube add 5 mL of solution B and 10 mL of solution C, shake for 45 seconds and allow to stand at room temperature for 30 minutes, add 20 mL of dichloromethane and shake vigorously for 1 minute; centrifuge and use the aqueous layer.<\/p>\n

(4) To 5 mL of a solution containing 0.00012% of sodium alendronate BPCRS in solution A in a screw cap centrifuge tube, add 5 mL of solution B and 10 mL of solution C, shake for 45 seconds and allow to stand at room temperature for 30 minutes. Add 20 mL of dichloromethane and shake vigorously for 1 minute, centrifuge and use the aqueous layer.<\/p>\n

CHROMATOGRAPHIC CONDITIONS<\/p>\n

(a) Use a stainless steel column (25 cm \u00d7 4.1 mm) packed with styrene-divinylbenzene copolymer (10 \u03bcm) (Hamilton PRP-1 is suitable).<\/p>\n

(b) Use gradient elution and the mobile phase described below.<\/p>\n

(c) Use a flow rate of 1.8 mL per minute.<\/p>\n

(d) Use a column temperature of 45\u00b0.<\/p>\n

(e) Use a detection wavelength of 266 nm.<\/p>\n

(f) Inject 20 \u03bcL of each solution.<\/p>\n

MOBILE PHASE<\/p>\n

Mobile phase A 3 volumes of acetonitrile and 17 volumes of buffer solution.<\/p>\n

Mobile phase B 3 volumes of buffer solution and 7 volumes of acetonitrile.<\/p>\n\n\n\n\n\n\n\n
Time (Minutes) <\/strong><\/span><\/td>\nMobile phase A (% v\/v)<\/strong><\/span><\/td>\nMobile phase B (% v\/v) <\/strong><\/span><\/td>\nComment<\/strong><\/span><\/td>\n<\/tr>\n
0-15 <\/span><\/td>\n\u00a0100\u219250<\/span><\/td>\n0\u219250<\/span><\/td>\nlinear gradient<\/span><\/td>\n<\/tr>\n
15-25<\/span><\/td>\n\u00a050\u21920<\/span><\/td>\n50\u2192100<\/span><\/td>\nlinear gradient<\/span><\/td>\n<\/tr>\n
25-27<\/span><\/td>\n\u00a00\u2192100<\/span><\/td>\n100\u21920<\/span><\/td>\nlinear gradient<\/span><\/td>\n<\/tr>\n
27-32<\/span><\/td>\n\u00a0100<\/span><\/td>\n0<\/span><\/td>\nre-equilibration<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

The retention time of the peaks due to alendronic acid and aminobutanoic acid, as their derivatives, are about 5 minutes and about 9.5 minutes respectively.<\/p>\n

SYSTEM SUITABILITY<\/p>\n

The test is not valid unless, in the chromatogram obtained with solution (3), the resolution between the two principal peaks is at least 10.0.<\/p>\n

LIMITS<\/p>\n

In the chromatogram obtained with solution (1):<\/p>\n

the area of any peak corresponding to 4-aminobutanoic acid is not greater than the area of the corresponding peak in the chromatogram obtained with solution (2) (0.5%);<\/p>\n

the area of any other secondary peak is not greater than half the area of the principal peak in the chromatogram obtained with solution (4) (0.1%).<\/p>\n

Disregard any peak with an area less than 0.25 times the area of the principal peak in the chromatogram obtained with solution (4) (0.05%).<\/p>\n

Impurities B and C<\/h3>\n

Carry out the method for liquid chromatography, Appendix III D, using the following solutions.<\/p>\n

(1) To a quantity of the powdered tablets containing the equivalent of 0.1 g of alendronic acid, add 20 mL of water and mix with the aid of ultrasound for 30 minutes. Add sufficient water to produce 25 mL and filter (Whatman GF\/C is suitable).<\/p>\n

(2) 0.0024% w\/v of orthophosphoric acid (impurity B) and 0.002% w\/v of phosphorous acid (impurity C).<\/p>\n

CHROMATOGRAPHIC CONDITIONS<\/p>\n

The chromatographic conditions described under Dissolution may be used. Allow the chromatography to proceed for twice the retention time of the principal peak.<\/p>\n

When the chromatograms are recorded under the prescribed conditions, the relative retentions with reference to alendronic acid (retention time, about 17 minutes) are: impurity B, about 1.3 and impurity C, about 1.6.<\/p>\n

SYSTEM SUITABILITY<\/p>\n

The test is not valid unless, in the chromatogram obtained with solution (2), the signal-to-noise ratios of the peaks due to impurity B and impurity C are at least 10.<\/p>\n

LIMITS<\/p>\n

In the chromatogram obtained with solution (1):<\/p>\n

the area of any peak corresponding to impurity B or impurity C is not greater than the area of any corresponding peak in the chromatogram obtained with solution (2) (0.5%).<\/p>\n

ASSAY<\/h2>\n

Weigh and powder 20 tablets. Carry out the method for liquid chromatography, Appendix III D, using the following solutions.<\/p>\n

(1) Mix a quantity of the powdered tablets containing the equivalent of 50 mg of alendronic acid with 20 mL of water for 30 minutes with the aid of ultrasound and occasional shaking, and agitate until cool, add sufficient water to produce 25 mL, mix and filter (Whatman GF\/C is suitable).<\/p>\n

(2) 0.22% w\/v of sodium alendronate BPCRS.<\/p>\n

CHROMATOGRAPHIC CONDITIONS<\/p>\n

The chromatographic conditions described under Dissolution may be used.<\/p>\n

DETERMINATION OF CONTENT<\/p>\n

Calculate the content of C4<\/sub>H13<\/sub>NO7<\/sub>P2<\/sub> in the tablets using the declared content of C4<\/sub>H12<\/sub>NNaO7<\/sub>P2<\/sub> in sodium alendronate BPCRS. Each mg of C4<\/sub>H12<\/sub>NNaO7<\/sub>P2<\/sub> is equivalent to 0.9189 mg of C4<\/sub>H13<\/sub>NO7<\/sub>P2<\/sub><\/p>\n

LABELLING<\/h2>\n

The quantity of active ingredient is stated in terms of the equivalent amount of alendronic acid.<\/p>\n

IMPURITIES<\/h2>\n

The impurities limited by the requirements of this monograph include impurities A, B and C listed under Sodium Alendronate Trihydrate.<\/p>\n","protected":false},"excerpt":{"rendered":"

(Ph. Eur. 11.6 update) Action and use Bisphosphonate; treatment of osteoporosis. DEFINITION Alendronic Acid Tablets contain Sodium Alendronate Trihydrate. The tablets comply with the requirements stated under Tablets and with the following requirements. Content of alendronic acid, C4H13NO7P2 95.0 to 105.0% of the stated amount. IDENTIFICATION A. Carry out the method for thin-layer chromatography, Appendix…<\/p>\n","protected":false},"author":5,"featured_media":2824,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[175],"tags":[],"class_list":["post-2800","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-formulated-preparations-specific-monographs"],"acf":[],"_links":{"self":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/2800","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/users\/5"}],"replies":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/comments?post=2800"}],"version-history":[{"count":5,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/2800\/revisions"}],"predecessor-version":[{"id":10957,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/2800\/revisions\/10957"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/2824"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=2800"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=2800"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=2800"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}