Pliant Therapeutics, Inc., 160 Littlefield Ave, South San Francisco, CA 94020, United States.
Module 3 Pharmaceutical Consulting, P.O. Box 3032, Incline Village, NV 89450, United States.
J Pharm Sci. 2021 Jul;110(7):2590-2608.e56. doi: 10.1016/j.xphs.2021.03.017. Epub 2021 Mar 28.
This review identified 126 commercially available antibodies approved globally between 1986 and February 2021 including 10 antibody drug conjugates, 16 biosimilars, and 3 antibody fragments. Prior to 2014 there were ≤ 5 approved each year, but after 2014 there have been ≥ 7 approved each year with the years 2017, 2019 and 2020 having the most at 17 each. A total of 136 products were identified of which 36 are lyophilized powders and 100 are solutions. The routes of administration are mainly subcutaneous or intravenous infusion with three intravenous bolus, two intravitreal, and one intramuscular. The subcutaneous products are ready-to-use solutions or reconstituted lyophilized powders that do not require dilution while most intravenous products are concentrates that require dilution into saline or another intravenous fluid prior to infusion. Most are packaged in single-dose units and the exception of multi-use is Herceptin® and its biosimilars. The package configurations are vials, prefilled autoinjectors, or prefilled syringes. A typical antibody formulation contains an antibody, an excipient to adjust tonicity or osmolality for solutions or a lyoprotectant for lyophilized powders, a buffer, and a surfactant. The ionic tonicity-adjusting excipient is mainly sodium chloride and the non-ionic osmolality-adjusting excipients include sucrose, trehalose, mannitol, maltose, and sorbitol. The lyoprotectants are trehalose and sucrose. The pH range is 4.8-8.0 and the buffers or pH-modifying agents include histidine, citrate, succinate, acetate, phosphate, glutamate, adipic acid, aspartic acid, lactic acid, tromethamine, and 2-(N-morpholino)-ethanesulfonic acid. The surfactants include mostly polysorbate 20 or polysorbate 80, with four containing poloxamer 188, and one that does not contain a surfactant but contains PEG 3350. One product does not contain a buffer, and 12 do not contain a surfactant. The viscosity-lowering excipients are sodium chloride and the amino acids arginine, glycine, proline, and lysine. Arginine may also function to adjust ionic strength and minimize aggregation. Human serum albumin is used in 2 products for intravenous infusion. Other excipients include methionine as an anti-oxidant, and EDTA or DTPA as chelating agents. The maximum volume of subcutaneous injection is 15 mL administered over 3-5 minutes, but the typically volume is 0.5-2 mL. Five fixed-dose combinations have recently been approved and four contain hyaluronidase to assist the large volume subcutaneous injection of up to 15 mL, while one is a fixed-dose combination for intravenous with three antibodies. Prefilled autoinjectors and syringes are becoming more common and many come affixed with a needle of 27-gauge or 29-gauge, while a few have a 26-gauge or a 30-gauge needle. Recent advancements include hyaluronidase to assist the large subcutaneous injection volume of 5-15 mL, fixed-dose combinations, buffer-free formulation, and smaller subcutaneous injection volume (0.1 mL).
本综述确定了 1986 年至 2021 年 2 月期间在全球范围内批准的 126 种商业可获得的抗体,包括 10 种抗体药物偶联物、16 种生物仿制药和 3 种抗体片段。在 2014 年之前,每年批准的数量≤5 种,但自 2014 年以来,每年批准的数量≥7 种,2017 年、2019 年和 2020 年批准的数量最多,各有 17 种。共确定了 136 种产品,其中 36 种为冻干粉末,100 种为溶液。给药途径主要为皮下或静脉输注,其中 3 种为静脉推注,2 种为玻璃体内,1 种为肌内。皮下产品为即用型溶液或复溶冻干粉末,无需稀释,而大多数静脉产品为浓缩物,在输注前需要稀释到生理盐水或其他静脉液中。大多数产品采用单剂量单位包装,只有 Herceptin®及其生物仿制药为多剂量包装。包装形式为小瓶、预填充自动注射器或预填充注射器。典型的抗体制剂包含抗体、用于调整溶液的渗透压或等张性的赋形剂或用于冻干粉末的保护剂、缓冲液和表面活性剂。离子渗透压调节剂主要为氯化钠,非离子渗透压调节剂包括蔗糖、海藻糖、甘露醇、麦芽糖和山梨糖醇。保护剂为海藻糖和蔗糖。pH 值范围为 4.8-8.0,缓冲液或 pH 调节剂包括组氨酸、柠檬酸盐、琥珀酸盐、醋酸盐、磷酸盐、谷氨酸、己二酸、天冬氨酸、乳酸、三羟甲基氨基甲烷和 2-(N-吗啉)-乙磺酸。表面活性剂主要包括聚山梨酯 20 或聚山梨酯 80,其中 4 种含有泊洛沙姆 188,1 种不含表面活性剂但含有 PEG 3350。一种产品不含缓冲液,12 种产品不含表面活性剂。降低粘度的赋形剂为氯化钠和氨基酸精氨酸、甘氨酸、脯氨酸和赖氨酸。精氨酸也可能用于调节离子强度和最小化聚集。两种静脉输注产品中使用人血清白蛋白。其他赋形剂包括作为抗氧化剂的蛋氨酸和作为螯合剂的 EDTA 或 DTPA。皮下注射的最大体积为 15 毫升,注射时间为 3-5 分钟,但通常体积为 0.5-2 毫升。最近批准了 5 种固定剂量组合,其中 4 种含有透明质酸酶,以帮助 15 毫升大体积皮下注射,而 1 种是含有三种抗体的静脉固定剂量组合。预填充自动注射器和注射器越来越常见,许多注射器带有 27 号或 29 号针头,而少数带有 26 号或 30 号针头。最近的进展包括透明质酸酶以帮助 5-15 毫升大体积皮下注射、固定剂量组合、无缓冲液配方和更小的皮下注射体积(0.1 毫升)。